Stimulator, Nerve, Peripheral, Electric (KOI) contract manufacturers
5 US facilities list FDA product code KOI as a contract manufacturer (5) or contract sterilizer (0).
FDA-registered (openFDA, export of Oct 21, 2026)
- FDA device name
- Stimulator, Nerve, Peripheral, Electric
- Product code
- KOI (FDA product classification database)
- Device class
- Class II
- Regulation
- 21 CFR 868.2775
- Classification panel
- Anesthesiology
Where they are
Pennsylvania 2 · Connecticut 1 · Minnesota 1 · New Jersey 1
All 5 facilities
| Company | FDA registration | Establishment type | Device categories | City and state | Certification | Updated |
|---|---|---|---|---|---|---|
| Defibtech Branford | 3012972516 | Contract manufacturer | Anesthesiology; Cardiovascular | Branford, CT | Not verified | Oct 21, 2026 |
| MINDRAY DS USA, Inc. | 2221819 | Contract manufacturer | Cardiovascular; Anesthesiology; Neurology +4 more | Mahwah, NJ | Not verified | Oct 21, 2026 |
| NORTECH SYSTEMS, INC. | 2183613 | Contract manufacturer | Anesthesiology; Cardiovascular; Gastroenterology and urology +6 more | Milaca, MN | Not verified | Oct 21, 2026 |
| Philips North America LLC | 3012528160 | Contract manufacturer | Cardiovascular; Anesthesiology; General hospital +2 more | Murrysville, PA | Not verified | Oct 21, 2026 |
| Philips North America LLC | 3016701404 | Contract manufacturer | Cardiovascular; Anesthesiology; General hospital +2 more | Export, PA | Not verified | Oct 21, 2026 |
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