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Sign in to claim this brandCPM Medical Consultants, LLC
US
Last updated September 17, 2026
What CPM Medical Consultants, LLC makes
CPM Medical Consultants, LLC manufactures a range of orthopedic implants including cruciate-retaining and posterior-stabilized total knee prostheses, a ceramic-on-polyethylene total hip prosthesis, spinal bone screws and internal fixation system rods, reusable joint implantation kits, reusable knee tibia prosthesis trial instruments, and orthopaedic bone screws that are non‑sterile and non‑bioabsorbable. Specific product lines include the STERIZO Total Knee and Hip Systems, the Fuse ULTRA Foot Plating System, the Fuse Pedicle Screw System, and the Tibial Revision Platform.
The company's devices are classified as Class I or Class II medical devices and are listed in the FDA UDI database. CPM Medical Consultants, LLC is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does CPM Medical Consultants, LLC manufacture?
CPM Medical Consultants, LLC manufactures orthopedic implants such as cruciate-retaining and posterior-stabilized total knee prostheses, ceramic-on-polyethylene total hip prostheses, spinal bone screws, internal fixation system rods, reusable joint prosthesis implantation kits, reusable knee tibia prosthesis trials, and non-sterile, non-bioabsorbable orthopaedic bone screws. Specific product lines include the STERIZO Total Knee and Hip Systems, Fuse ULTRA Foot Plating System, Fuse Pedicle Screw System, and Tibial Revision Platform.
Where is CPM Medical Consultants, LLC based?
CPM Medical Consultants, LLC is based in the United States, as stated in the company's summary and country field within the provided device data.
In which regulatory registry are CPM Medical Consultants, LLC's devices listed?
The devices manufactured by CPM Medical Consultants, LLC are listed in the FDA UDI database, which is the Unique Device Identification system maintained by the U.S. Food and Drug Administration for tracking medical devices.
How are the devices manufactured by CPM Medical Consultants, LLC classified?
The devices manufactured by CPM Medical Consultants, LLC are classified as either Class I or Class II medical devices, indicating varying levels of regulatory control based on risk, with Class II devices requiring special controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
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 2 of 30| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev B | 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 | M-3311-2050 | 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 Pedicle Screw System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev C | FDA UDI | Class II | Active |
| Fuse Pedicle Screw System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | R326920-T | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA FOOT PLATING SYSTEM | OS422514 | 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 Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | M-3301-4065 | 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 |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| Orbitum VI Staple | 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 Hip System | Rev A | FDA UDI | Class II | Active |
| Fuse ULTRA Foot plating System | R421728 | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| Orbitum Staple System | Rev A | FDA UDI | Class II | Active |
| Fuse Pedicle Screw 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 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 C | FDA UDI | Class II | Active |
| Orbitum X Staple | FO-2013-209 | 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 Hip System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | Rev A | FDA UDI | Class II | Active |
| STERIZO Total Knee System | M-3311-2020 | FDA UDI | Class II | Active |
| STERIZO Total Hip System | Rev A | FDA UDI | Class II | Active |
| Tibial Revision Platform | Rev A | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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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.
There is 1 recall record for CPM Medical Consultants, LLC, initiated on 2025-09-17, with statuses recorded as open and classified. The reason given is that the instructions for use for a foot plating system are being updated to remove a sterilization requirement of 3 minutes exposure at 134-137°C (273-279°F) and 40 mBar for 5-10 minutes drying time, as these requirements do not apply in the United States.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| 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. |