Contract manufacturerJEDMED Instrument Company (Saint Louis, MO)MissouriEar, nose and throatClass I
JEDMED Instrument Company
Contract manufacturer ยท Saint Louis, MO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1926681 (openFDA record; or search FDA's registration database)
- FEI number
- 1926681
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- JEDMED INSTRUMENT CO. (FDA owner/operator no. 1926681)
- Registered address
- 5416 JEDMED CT., Saint Louis, MO 63129
- Contract listings
- 3 device listings, 3 product codes, first listed Oct 29, 1982
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| KAE | Forceps, Ent | Class I | Ear, nose and throat | Contract manufacturing | Oct 29, 1982 |
| KTG | Knife, Ent | Class I | Ear, nose and throat | Contract manufacturing | Jun 10, 2016 |
| LRC | Instrument, Ent Manual Surgical | Class I | Ear, nose and throat | Contract manufacturing | Sep 15, 2015 |