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US
Last updated September 17, 2026
What MAXX ORTHOPEDICS INC. makes
Maxx Orthopedics Inc. manufactures orthopedic implants for knee and hip replacements, including polyethylene tibial components, metallic femoral prostheses, acetabular liners, tibial inserts, and modular hip stems. Their portfolio includes uncoated and coated knee and hip implants, as well as press-fit femoral stems designed for total joint arthroplasty.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. Maxx Orthopedics Inc. 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 Maxx Orthopedics Inc. manufacture?
Maxx Orthopedics Inc. specializes in orthopedic implants used primarily for knee and hip replacements. Their product line includes uncoated and coated knee tibia and femur prostheses (both metallic and polyethylene), non-constrained polyethylene acetabular liners, tibial inserts, and modular hip femur prostheses. These devices are designed to restore joint function in patients undergoing total joint arthroplasty.
Where is Maxx Orthopedics Inc. based?
Maxx Orthopedics Inc. is headquartered in the United States. The company’s location is relevant for regulatory oversight, manufacturing standards, and compliance with U.S. medical device regulations.
Which regulatory registries or databases list Maxx Orthopedics Inc.’s devices?
Maxx Orthopedics Inc.’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and patients to verify device details and compliance.
How are Maxx Orthopedics Inc.’s devices classified under FDA regulations?
All of Maxx Orthopedics Inc.’s devices fall under Class II classification by the FDA. This classification applies to devices that generally pose moderate risk and require special controls (beyond general controls) to ensure safety and effectiveness, such as orthopedic implants that require performance standards or post-market surveillance.
What distinguishes Maxx Orthopedics Inc.’s orthopedic implants from other manufacturers?
Maxx Orthopedics Inc. focuses on a range of modular and press-fit orthopedic implants, including both knee and hip replacements, with variations like uncoated/metallic polyethylene components and modular hip stems. Their devices are designed for durability and compatibility in total joint arthroplasty, with a consistent classification as Class II, indicating they undergo rigorous evaluation for structural integrity and clinical performance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 2460 General Armistead Ave, Norristown, PA, 19403
- Website
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3007311878
- DUNS Number
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Catalogue (4380)
Page 79 of 88| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Libertas | MO-CCNG-43/22 | FDA UDI | Class II | Active |
| Freedom | ATUCLF812-AK | FDA UDI | Class II | Active |
| Freedom | ATUCLE509-AK | FDA UDI | Class II | Active |
| Libertas | MO-CIND-59/40 | FDA UDI | Class II | Active |
| Freedom | ALCRXH817-K | FDA UDI | Class II | Active |
| Freedom | ATUCLB211-AK | FDA UDI | Class II | Active |
| Freedom Pck | RLPSXF531-RK | FDA UDI | Class II | Active |
| Freedom | ATMCRG511-AK | FDA UDI | Class II | Active |
| Freedom Knee | ALPSXD214-K | FDA UDI | Class II | Active |
| Freedom | ATMCLH610-AK | FDA UDI | Class II | Active |
| Libertas | MO-CCNG-53/32 | FDA UDI | Class II | Active |
| Libertas | MO-BABK-51/28 | FDA UDI | Class II | Active |
| Freedom | MLUCXF709-K | FDA UDI | Class II | Active |
| Libertas | MO-CONG-62/36 | FDA UDI | Class II | Active |
| Libertas | MO-MLLE-MD/28 | FDA UDI | Class II | Active |
| Freedom | LLPSXD109-ML | FDA UDI | Class II | Active |
| Libertas | MO-COND-66/40 | FDA UDI | Class II | Active |
| Freedom | ATMCLG817-AK | FDA UDI | Class II | Active |
| Freedom | MLMCLE514-K | FDA UDI | Class II | Active |
| Freedom Knee | MLPSXC309-K | FDA UDI | Class II | Active |
| Freedom | ATPSLC112-AK | FDA UDI | Class II | Active |
| Libertas | MO-CONG-58/36 | FDA UDI | Class II | Active |
| Libertas | MO-STRC-28/18 | FDA UDI | Class II | Active |
| Libertas | MO-SFDC-32/15 | FDA UDI | Class II | Active |
| Freedom | DURMLL309-UK | FDA UDI | Class II | Active |
| Freedom | ATMCRG509-AK | FDA UDI | Class II | Active |
| Freedom Stemmed | RSUU2200-RK | FDA UDI | Class II | Active |
| Freedom | MLMCLE512-K | FDA UDI | Class II | Active |
| Libertas | MO-CFND-48/28 | FDA UDI | Class II | Active |
| Freedom | ATMCRG520-AK | FDA UDI | Class II | Active |
| Freedom Knee | MTUUX800-K | FDA UDI | Class II | Active |
| Freedom | BTLMRL200-UK | FDA UDI | Class II | Active |
| Freedom | ATPSLG610-AK | FDA UDI | Class II | Active |
| Freedom | ATPSLC311-AK | FDA UDI | Class II | Active |
| Libertas | MO-MLAD-44/28 | FDA UDI | Class II | Active |
| Libertas | MO-SFCC-28/13 | FDA UDI | Class II | Active |
| Libertas | MO-STCM-00/03 | FDA UDI | Class II | Active |
| Libertas | MO-HDAM-22/35+ | FDA UDI | Class II | Active |
| Libertas | MO-MLUE-MD/32 | FDA UDI | Class II | Active |
| Freedom | UFPSLD00-GK | FDA UDI | Class II | Active |
| Libertas | MO-STVC-25/00 | FDA UDI | Class II | Active |
| Freedom | UFCRLE00-GK | FDA UDI | Class II | Active |
| Libertas | MO-STTC-28/11 | FDA UDI | Class II | Active |
| Freedom | ALCRXB114-K | FDA UDI | Class II | Active |
| Freedom | ATMCLG609-AK | FDA UDI | Class II | Active |
| Freedom | MLMCRD514-K | FDA UDI | Class II | Active |
| Libertas | MO-CLND-68/36 | FDA UDI | Class II | Active |
| Libertas | MO-MSBC-60/52 | FDA UDI | Class II | Active |
| Freedom | ATPSLF517-AK | FDA UDI | Class II | Active |
| Freedom Knee | MLUCXA113-K | FDA UDI | Class II | Active |
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