Contract manufacturerANSEN CORPORATION (Ogd, NY)New YorkCardiovascularClass III
ANSEN CORPORATION
Contract manufacturer · Ogd, NY
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3003867964 (openFDA record; or search FDA's registration database)
- FEI number
- 3003867964
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- ANSEN CORPORATION (FDA owner/operator no. 9037108)
- Registered address
- 100 CHIMNEY POINT DR., Ogd, NY 13669
- Contract listings
- 2 device listings, 1 product codes, first listed Jan 31, 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 |
|---|---|---|---|---|---|
| MKJ | Automated External Defibrillators (Non-Wearable) | Class III | Cardiovascular | Contract manufacturing | Jan 31, 2007 |