For shops · ISO 13485 / FDA-registered medical shops
ISO 13485 medical shops: implant and instrument RFQs routed to you
Medical device buyers need the quality system before they need the quote. If your shop holds ISO 13485 and runs biocompatible materials, we route the RFQs that match.
RFQs on the board
Medical device RFQs on our board
Orthopedic and dental implants
- Bone screws, plates, cages, and dental abutments in Ti-6Al-4V ELI (Grade 23)
- Cobalt-chrome (CoCrMo, ASTM F75) joint replacement geometry
- Full traceability from mill to packaging, electropolish partner required
Surgical instruments and hand-pieces
- Reamers, drivers, retractors in 17-4 PH, 455 stainless, PEEK
- Swiss and 5-axis milled parts with surface finishes called out
- Passivation per ASTM A967 standard
Housings, enclosures, and injection-molded parts
- Diagnostic equipment and point-of-care device housings in 6061 and medical polymers
- Insulin pump, infusion, and monitoring housings
- Prototype 1–50 with path to production
Biocompatible polymer parts
- PEEK, UHMWPE, Delrin medical grade, and PPSU parts
- Validated sterilization paths (gamma, EtO) noted on RFQ
What qualifies you
What a qualified medical shop looks like
- ISO 13485 (current)
- Documented in your profile with scope and the registrar.
- FDA facility registration
- If you handle finished devices or regulated components. Not required for all RFQs; call out your scope.
- Material biocompatibility
- Implant-grade Ti-6Al-4V ELI, CoCrMo per ASTM F75, 316LVM, 455 and 17-4 PH stainless, medical polymers with full certs.
- Finishing partners
- Electropolish, passivation, and glass-bead that meet medical cleanliness. In-house or named vendor.
- Validated processes
- Where the device requires IQ/OQ/PQ, say so on your profile with the processes you have validated.
- Lot traceability
- Material heat lot tied to serial-numbered parts; retention sample program.
- Cleanroom (helps)
- ISO Class 7 or 8 cleanroom assembly or packaging for implants and sterile devices.
What you get
What a medical partner gets
Cert-matched RFQs only
ISO 13485 RFQs go only to ISO 13485 shops. We do not send you non-regulated work to pad the stream.
Realistic schedules
Medical FAI and sterilization lead time is set with the buyer up front; you quote the time you can hit.
Free to join; no fees
No subscription, no per-RFQ fee, no commission on your price.
Material fronted
Customer pays us before you cut; implant-grade stock on long lead is covered.
Keep your own customers
Our RFQs are from new medical device buyers we bring in; we do not approach your existing accounts.
Common questions
The pushback we hear, answered
Where the RFQs come from
The buyer pages that attract this work
These are the capability, material, and industry landing pages buyers find on Google and in AI search. RFQs from them land in our inbox and route to the matching shops.
Add ISO 13485 to your profile and we route the matching medical RFQs
Flag ISO 13485, FDA registration, and the biocompatible materials you handle. The next matching medical device RFQ comes to you.