Contract manufacturerHYDROFERA, LLC. (Manchester, CT)ConnecticutGeneral and plastic surgeryEar, nose and throatUnclassifiedClass I
HYDROFERA, LLC.
Contract manufacturer ยท Manchester, CT
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1225532 (openFDA record; or search FDA's registration database)
- FEI number
- 3001236237
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- HYDROFERA, LLC. (FDA owner/operator no. 9028346)
- Registered address
- 340 Progress Drive, Manchester, CT 06042
- Contract listings
- 6 device listings, 6 product codes, first listed Mar 24, 1998
- 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 |
|---|---|---|---|---|---|
| EFQ | Gauze/Sponge, Internal | Unclassified | General and plastic surgery | Contract manufacturing | Jan 28, 2008 |
| EMX | Balloon, Epistaxis | Class I | Ear, nose and throat | Contract manufacturing | Mar 24, 1998 |
| GDY | Gauze/Sponge, Internal, X-Ray Detectable | Class I | General and plastic surgery | Contract manufacturing | Jun 21, 2018 |
| KCN | Ear Wick | Class I | Ear, nose and throat | Contract manufacturing | Jul 3, 2018 |
| MDM | Instrument, Manual, Surgical, General Use | Class I | General and plastic surgery | Contract manufacturing | Dec 9, 2011 |
| NAB | Gauze / Sponge,Nonresorbable For External Use | Class I | General and plastic surgery | Contract manufacturing | Dec 9, 2011 |