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Sign in to claim this brandCPM Medical Consultants, LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 4343 Sigma Road, Farmers Branch, TX, 75244
- Website
- xx.xx
- —
- —
- [email protected]
- Phone
- 972-331-5860
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3007334927
- DUNS Number
- 017138000
Catalogue (1498)
Page 1 of 30| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fuse ULTRA Foot plating System | R421818 | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | R421835 | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | M-3301-4073 | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | OS328026 | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | OS327936 | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev D | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | OS421824 | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev D | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA FOOT PLATING SYSTEM | OS422614 | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | FZ-I-050 | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA FOOT PLATING SYSTEM | OS2013166 | FDA UDI | Class I | Active |
| Fuse Pedicle Screw System | Rev D | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev D | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | R326955-T | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | REV A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | OS421006R | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | 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 17, 2025 | Z-0230-2026 | — | open, classified | Instructions for use for a foot plating system is being updated to remove the second option of requirements for sterilization which was 3 minutes exposure time at 134-137-degrees C (273-279-degrees F) and 40mBar for 5-10 minutes drying time, because these requirements do not apply in the United States. |