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Sign in to claim this brandGYNEX CORPORATION
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 6631 Browning Dr, North Richland Hills, TX, 76180
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3001238683
- DUNS Number
- 012997685
Catalogue (495)
Page 1 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Gynex | 4950 | FDA UDI | Class I | Active |
| Gynex | 3585-27 | FDA UDI | Class I | Active |
| Gynex | TT007 | FDA UDI | Class I | Active |
| Gynex | 2525 | FDA UDI | Class I | Active |
| Gynex | 2781 | FDA UDI | Class I | Active |
| Gynex | 2805 | FDA UDI | Class I | Active |
| Gynex | TT032 | FDA UDI | Class I | Active |
| Gynex | TT585-21 | FDA UDI | Class I | Active |
| Carrera Loop Electrodes | CMR-2010 | FDA UDI | Class II | Active |
| Gynex | 1029 | FDA UDI | Class I | Active |
| Gynex | 3596 | FDA UDI | Class I | Active |
| Gynex | 1200 | FDA UDI | Class I | Active |
| Gynex | 3580 | FDA UDI | Class I | Active |
| Gynex | TT595-30 | FDA UDI | Class I | Active |
| Gynex | PH-99 | FDA UDI | Class I | Active |
| Gynex | 3685-23 | FDA UDI | Class I | Active |
| Radius Loop Electrodes | 12-2015 | FDA UDI | Class II | Active |
| Angle Hook | 3225 | FDA UDI | Class II | Active |
| Gynex | 3314 | FDA UDI | Class I | Active |
| LLETZ Emmett Tenaculum | 3240 | FDA UDI | Class II | Active |
| Gynex | 2430 | FDA UDI | Class I | Active |
| Gynex | 14-1020 | FDA UDI | Class II | Active |
| Gynex | 3590-27 | FDA UDI | Class I | Active |
| Gynex | 4005.4 | FDA UDI | Class I | Active |
| Gynex | TT0525 | FDA UDI | Class I | Active |
| Gynex | 3584 | FDA UDI | Class I | Active |
| Gynex | 3598 | FDA UDI | Class I | Active |
| Gynex | TT580-30 | FDA UDI | Class I | Active |
| Gynex | 3590 | FDA UDI | Class I | Active |
| Carrera Loop ELectrodes | CMR-1010 | FDA UDI | Class II | Active |
| Gynex | 2883 | FDA UDI | Class I | Active |
| Gynex | NHL3450 | FDA UDI | Class I | Active |
| Gynex | 530LVCDA-R | FDA UDI | Class II | Active |
| Gynex | 3556 | FDA UDI | Class I | Active |
| Carrera Loop Electrodes | OCMR-2015 | FDA UDI | Class II | Active |
| Patient Dispersive Pad | 33-714 | FDA UDI | Class II | Active |
| Gynex | 3010 | FDA UDI | Class I | Active |
| Gynex | 4212 | FDA UDI | Class I | Active |
| Gynex | 3595-30 | FDA UDI | Class I | Active |
| Gynex | 1325 | FDA UDI | Class I | Active |
| Gynex | TT580-27 | FDA UDI | Class I | Active |
| Gynex | 1200-15 | FDA UDI | Class I | Active |
| Gynex | 2778 | FDA UDI | Class I | Active |
| Gynex | 3205 | FDA UDI | Class I | Active |
| Gynex | 2875 | FDA UDI | Class I | Active |
| Radius Loop Electrodes | 12-0505 | FDA UDI | Class II | Active |
| Gynex | 2845 | FDA UDI | Class I | Active |
| Gynex | 14-1015 | FDA UDI | Class II | Active |
| Electrode Handpiece, Foot Activated | 950 | FDA UDI | Class II | Active |
| LiteTouch Braun Tenaculum | T2230 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 6, 2012 | Z-0008-2013 | — | terminated | The wrong electrical connector pin was attached to the cord during assembly by the manufacturer. this electrical connector is too big to fit into the port on the foot activated generator. this makes the device unusable. |