Your brand of lift recliners — engineered, built and certified under one roof.
Since 2017 we’ve manufactured private-label power lift recliners for retail, e-commerce, medical and bariatric distributors in 30+ countries. Low MOQ, a medical-grade quality system, and full export documentation — so you can launch under your own brand with confidence.

Since 2017
Lift Chair Factory
8,000㎡
Production Floor
2,500/mo
Monthly Capacity
30+
Countries Served
A factory partner built for distributors, not just orders.
Low MOQ, no gatekeeping
Start with 10 units per in-catalog model, 20 for custom builds, and from a single unit on the bariatric line. Small first orders are welcome.
Medical-grade quality
ISO 13485-aligned QMS, a 6-step QC process, and long-life TiMotion motor systems — built to pass your market’s inspections.
Export-ready documents
CE Declaration of Conformity, RoHS reports, FDA registration, biocompatibility, and IFU in your market language — supplied pre-PO.
Six layers of customization — your brand, end to end.
01 · Logo & branding
Your logo on the chair, packaging, IFU and warranty card. We ship under your brand — never ours.
02 · Fabric & color
Chenille, faux leather or top-grain leather in your color palette. Material grade tuned to your price point.
03 · Packaging & IFU
Branded cartons, inserts, instruction manuals and warranty cards in your market’s language.
04 · Feature configuration
Motor count, heating, massage, USB & Type-C charging, headrest and lumbar options — built to your spec.
05 · Market localization
Voltage, plug type, multi-language hand control and the certifications your destination requires.
06 · Exclusive silhouette
Co-develop a new frame or silhouette locked to your brand — exclusivity typically 24–36 months.
A 7-step process built for predictability.
- 1
Brief & spec
You send requirements — or use our spec sheet template so nothing gets lost in translation.
- 2
Quote & timeline
Itemized quote and production timeline back to you within 24 hours.
- 3
Sample
Refundable sample fee. Branded pre-production sample in about 7 days.
- 4
Spec lock
You sign off a binding spec sheet — the single source of truth for the run.
- 5
Production
Scheduled build with during-production (DUPRO) in-line quality checks.
- 6
Final QC & docs
6-step QC, plus your pre-PO documentation dossier compiled for customs.
- 7
Shipment
FOB, CIF, DDP or DAP. Full container (20’/40’/40HC) or LCL consolidation.
Low minimums, clear timelines.
| Order type | MOQ | Typical lead time |
|---|---|---|
| In-catalog model (your branding) | 10 units / model | ~30–40 days |
| Custom build (to your spec) | 20 units / model | ~45–60 days |
| Bariatric line | from 1 unit | ~40–50 days |
| Branded sample | 1 unit | ~7 days |
Sample fees are refundable against your first production order. Lead times are confirmed and binding after spec lock.
Your pre-PO documentation dossier.
- ISO 13485 certificate
- CE Declaration of Conformity
- RoHS test reports
- FDA establishment registration (US)
- Biocompatibility statements (where relevant)
- IFU in your market language
- Warranty terms
- Packaging dimensions & carton specs
Questions OEM buyers actually ask.
What’s the minimum order to start an OEM project?
MOQ is just 10 units per model for our in-catalog designs and 20 units for custom builds developed to your spec; our bariatric line is available from a single unit. There’s no volume tier or gatekeeping — small first orders are welcome.
How does OEM differ from private label in your terminology?
We use OEM to mean any production we manufacture for your brand, regardless of customization depth. Private label is the subset where the chair carries your branding (logo, packaging, IFU) but uses our existing chassis. Co-developed exclusive lines are private label + new chassis or silhouette locked to your brand for an agreed period.
Can you co-develop a chair that’s exclusive to our brand?
Yes. Co-developed exclusive lines (new silhouette, frame, or feature set locked to your brand) are available for committed brand partners. Development cost is shared, IP arrangements are negotiated up front, and exclusivity period is typically 24–36 months.
What documentation do you supply for our market?
Pre-PO dossier includes: ISO 13485 cert, CE Declaration of Conformity, RoHS test reports, FDA establishment registration (US), biocompatibility statements where relevant, IFU in your market language, warranty terms, and packaging dimensions.
Do you ship globally?
Yes — we routinely ship to US, EU, UK, Australia, Middle East (GCC), and Japan. Incoterms FOB Shanghai/Ningbo by default; CIF, DDP, and DAP available on request. Full container (20’/40’/40HC) and LCL (consolidated) shipping supported.