Order OEM Manufacturing

The product categories below ship out of our facilities every week under our own brand and under client OEM agreements. If your brand vision sits in one of these categories, we can quote production from week one – most of the underlying engineering, certification and tooling is already done.

Cryotherapy chambers. Whole-body electric cryotherapy chambers, hybrid nitrogen/electric systems and cold-air cryosaunas. Single-user and multi-user configurations. Operating temperatures from -85°C to -140°C. This is our core specialization – as a dedicated cryotherapy chamber manufacturer (and one of the few cryo chamber manufacturers operating outside Asia at this scale), we manufacture more units per year than most US competitors combined, and the engineering on the refrigeration stack has been refined over twenty-five years of production runs.

Localized cryotherapy machines. Cryo facial machines, cryo slimming devices, electric localized cryotherapy, contrast-temperature devices for medspa and aesthetic applications. Smaller form factor, faster certification paths, lower per-unit cost. Strong category for emerging brands entering the cryotherapy market.

Red light therapy equipment. Full-body red light therapy beds (660nm + 850nm dual-wavelength), red light loungers, infrared chambers and integrated multi-wavelength systems. Commercial-grade LED arrays, real measured irradiance at the treatment surface, full FDA Class II pathway support for clients positioning into the medical-device space. As a dedicated red light therapy manufacturer and recovery equipment manufacturer, we ship to brands across the US, EU, UK, Canada and APAC regions.

Longevity capsules and multi-modality recovery systems. Integrated longevity equipment combining halotherapy, red light, oxygen breathing, AI-guided breathwork, vibrational therapy and zero-gravity reclining seating. The Revique HaloX™ reference product on our site is one example – the underlying platform supports custom configurations for clients building specific longevity-brand identities.

Vacu-infrared training equipment. Treadmills and stationary bikes with vacuum/anti-gravity chambers and infrared heating. The vacu-cryo-infrared category specifically – Bodyshape, vacutherm, vacu-treadmills, vacu-bikes. Patented engineering, established commercial reliability, strong category for body-shaping and weight-loss-positioned brands.

Lymphatic massage rollers and wood-roller equipment. Full-body lymphatic massage roller machines, wood-roller bodyshaping systems with infrared and collagen light integration. Comparable category to Studio Figura’s Roll Shaper, manufactured at our facility under brand-owned configurations for regional wellness chains.

Coolsculpting-class body shapers and vacuum rollers. Vacuum-roller systems comparable to LPG Endermologie and Icoone, HIFEM-based muscle stimulation equipment in the Emsculpt-comparable category, and cryo-vacuum hybrid roller systems. Cosmetic-device-grade engineering for medspa-channel brands.

Massage chairs and de-stress furniture. Commercial-grade SL Track full-body massage chairs with 3D/4D roller systems, zero gravity recline, body scan and heat therapy. Lower-MOQ alternative to the consumer-focused Osaki, Bodyfriend and Inada brands for B2B wellness facility supply chains.

Access control kiosks and facial recognition terminals. Biometric access control kiosks with facial recognition, thermal scanning and gate relay control. Appropriate for 24/7 gym chains, wellness facility access management and corporate wellness suites.

Commercial wellness facility furniture. Custom reception desks, lounge seating, retail display units, locker systems and treatment-room cabinetry coordinated with the rest of the equipment supply. Useful when a brand wants its entire facility interior to ship from a single manufacturing partner.

Outside these categories, we evaluate custom manufacturing requests case by case – generally yes if the product sits in the wellness/recovery/biohacking space and matches our engineering capability, generally no if it sits in unrelated categories where another specialist manufacturer would serve you better.

The case for sourcing from China is unit cost. Nothing else. For commodity products at very high volumes, the math is strong and we wouldn’t argue against it. For premium wellness equipment manufactured in quantities of 50 to 5,000 units a year – which is the realistic volume range for almost every brand we work with – the calculation flips, and it flips for specific operational reasons rather than vague quality claims.

Intellectual property holds up. The honest version is that IP protection in China is improving but remains genuinely difficult to enforce for foreign brands at production scales below 50,000 units. We see this constantly – brands arrive after a Chinese factory began producing a near-clone of their equipment, sometimes through the same factory, sometimes through “former employees” who left and opened a competing operation a quarter later. European and US manufacturing operates under enforceable IP regimes. We sign IP-assignment agreements that mean something legally, and our supply chain is internal rather than distributed across factories where security is harder to control.

Lead times are reliable when something changes mid-production. Ocean freight from China to the US is 30-45 days minimum, before customs clearance. A mid-production engineering change order takes 8-12 weeks to propagate through a Chinese supply chain. European and North American production cycles that change order in 2-3 weeks. When a brand is racing to make a Q3 trade show, fix a design flaw discovered in user testing, or pivot a feature based on early customer feedback, the lead-time difference between continents directly determines whether the brand makes its window or misses it.

Communication doesn’t drop signal. Brands building premium wellness equipment ask precise engineering questions – surface irradiance at specific points, refrigerant operating curves, control software architecture, certification documentation lineage. Those conversations work better when the engineering team operates in English, in compatible time zones, and within cultural frames that match the brand’s expectations of communication transparency. The brands we work with consistently mention this as one of the operational factors that compounds across a multi-year relationship.

Customs and certification are simpler. CE-marked equipment manufactured in Europe ships into the EU and EFTA without import compliance overhead. US-finished equipment shipped within the US continental market doesn’t trigger import duties or FDA import alerts. Both of those reduce per-unit landed cost in ways that don’t show up on a comparison spreadsheet but show up on the bottom line at end of year.

Specific competitive context: ShineNova, Kaiyan Medical, Rlab and similar Asian OEM partners offer aggressive pricing on red light therapy and cryo equipment. CryoBuilt and CryoPhit USA offer North American manufacturing of cryotherapy systems. CryoMed sro manufactures cryosaunas out of Europe. The market has good options, and we don’t suggest otherwise. The argument for choosing Cryonick is specific to the operational profile a buyer needs: low MOQ, IP-sensitive engineering, premium-tier construction, fast iteration cycles and a service relationship that survives the second and third years of the partnership rather than degrading after the first production run.

“How do you actually protect my IP?”

Mutual NDAs are signed before substantive technical conversation. IP-assignment clauses in the manufacturing agreement transfer specific design rights to your brand. Engineering files are version-controlled and access-restricted to project staff. Production runs in our facilities rather than subcontracted to outside factories. We retain no rights to brand-specific configurations, branding elements or customer-developed features. For brands with high-IP-sensitivity products, we’ll sign whatever supplemental confidentiality and exclusivity agreements your counsel drafts – we’ve never had a brand walk away from the legal stage because of contractual disagreements about IP.

“Can you handle FDA Class II / CE / FCC / UL certification?”

Yes for CE – our engineering team handles CE documentation as part of standard production. For FDA Class II 510(k) clearance, we provide the technical documentation, prototype testing support, and engineering files your regulatory consultant needs to file. We don’t act as the formal regulatory sponsor – that role belongs to the brand owner – but the technical work that supports it ships from our facility. FCC and UL certification for specific markets are handled through partner labs on a project-cost basis.

“What’s your typical lead time?”

ODM with branded customization on existing platforms: 8-12 weeks from contract to first shipment. OEM production to your engineering drawings: 12-20 weeks. Full product development: 9-18 months for first production batch. These are realistic ranges, not aspirational ones. Brands that need faster than these timelines should expect to pay 25-50% premiums for expedited production slots.

“Can you ship internationally?”

Yes. Worldwide shipping handled through our logistics partners. CE-marked equipment ships freely within the EU and EFTA. US-manufactured units ship within North America without import duty. International customs documentation, packaging for ocean freight or air freight, and delivery to your warehouse or fulfillment center are all handled as part of standard project scope.

“Do you sign exclusivity agreements?”

For specific product categories, in specific markets, for limited terms – yes. We don’t sign global open-ended exclusivity that would lock us out of manufacturing for other brands in the category, because that’s not how OEM economics work. We do sign market-specific and product-specific exclusivity where the volume commitment supports it. Brands serious about exclusivity typically structure it as a tiered commitment – they get exclusivity in a defined geography in exchange for a guaranteed minimum annual volume.

“What happens if I want to move production after a few years?”

The brand keeps the IP. Engineering files, certification documentation, tooling specifications transfer with you. We don’t lock brands into permanent supply relationships – if you outgrow us, if your strategy changes, if you decide to insource production, the relationship ends cleanly. The brands that stay with us long term do so because the relationship continues to make sense, not because they’re contractually trapped.

“Are you actually larger than the Chinese factories quoting against you?”

No. Shenzhen factories like ShineNova and Kaiyan operate at volumes we don’t match for commodity red light therapy panels or basic infrared equipment. They’re excellent partners for that product profile. We compete on a different dimension – premium-tier wellness equipment, low-MOQ flexibility, IP-sensitive engineering, integrated multi-product fleets for wellness facility brands. If your volume forecast is 50,000 LED panels a year, talk to Shenzhen. If your volume forecast is 200 cryotherapy chambers a year and you need them branded, certified and IP-protected, talk to us.

“Can we visit your facility?”

Yes, by appointment. Most pre-contract conversations happen via video call because they’re more efficient, but qualified brands at the contract stage typically schedule a facility visit before signing larger commitments. We coordinate visits to whichever production location matches the project – Los Angeles for North American manufacturing relationships, European facilities for EU-positioned brands.