Contract manufacturerPEPIN MFG., INC. (Lake City, MN)MinnesotaAnesthesiologyGeneral and plastic surgeryNeurologyGeneral hospitalClass IIClass I
PEPIN MFG., INC.
Contract manufacturer ยท Lake City, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2132556 (openFDA record; or search FDA's registration database)
- FEI number
- 1000221051
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- PEPIN MFG., INC. (FDA owner/operator no. 9007792)
- Registered address
- 1875 HWY 61 SOUTH, Lake City, MN 55041
- Contract listings
- 7 device listings, 6 product codes, first listed Aug 10, 2007
- 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 |
|---|---|---|---|---|---|
| BZQ | Monitor, Breathing Frequency | Class II | Anesthesiology | Contract manufacturing | Sep 23, 2015 |
| FZP | Clip, Implantable | Class II | General and plastic surgery | Contract manufacturing | Mar 13, 2023 |
| GXY | Electrode, Cutaneous | Class II | Neurology | Contract manufacturing | Aug 10, 2007 |
| MKY | System, Skin Closure | Class I | General and plastic surgery | Contract manufacturing | Feb 3, 2023 |
| MNR | Ventilatory Effort Recorder | Class II | Anesthesiology | Contract manufacturing | Sep 23, 2015 |
| MZR | Topical Approximation System | Class I | General hospital | Contract manufacturing | Feb 3, 2023 |