Contract manufacturerSAUNDERS ELECTRONICS (South Portland, ME)MaineGeneral hospitalClass II
SAUNDERS ELECTRONICS
Contract manufacturer · South Portland, ME
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3013919529 (openFDA record; or search FDA's registration database)
- FEI number
- 3013919529
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Saunders Electronics (FDA owner/operator no. 10055706)
- Registered address
- 192 Gannett Drive, South Portland, ME 04106
- Contract listings
- 1 device listings, 1 product codes, first listed Aug 11, 2025
- 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 |
|---|---|---|---|---|---|
| QVY | Therapeutic Vibrational Mattress Pad, Adjunct Use In Neonatal Abstinence Syndrome Or Neonatal Opioid Withdrawal Syndrome | Class II | General hospital | Contract manufacturing | Aug 11, 2025 |