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US
Last updated May 23, 2026
What implantcast GmbH makes
The company produces reusable trial components for knee arthroplasty, including knee tibia and femur prosthesis trials, as well as tibial inserts and knee arthroplasty wedges. It also manufactures orthopaedic fixation tools such as press-fit femoral stems, broaches, and general internal orthopaedic fixation system implantation kits. Additional products include non-constrained polyethylene acetabular liners and specialized extension pieces, chisels, and extractors for femoral trials.
These devices are classified under FDA’s Class I and Class II regulatory categories and are listed in the FDA’s UDI (Unique Device Identification) database. The company operates from 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 implantcast GmbH manufacture?
implantcast GmbH specializes in reusable orthopaedic devices primarily used in knee arthroplasty procedures. Their product range includes trial components like knee tibia and femur prosthesis trials, tibial inserts, and knee arthroplasty wedges. They also produce orthopaedic fixation tools such as press-fit femoral stems, broaches, and implantation kits for general internal orthopaedic fixation. Additionally, they manufacture non-constrained polyethylene acetabular liners and specialized tools like extension pieces, chisels, and femoral trial extractors.
Where is implantcast GmbH based?
implantcast GmbH is based in the United States. The company’s location is relevant for regulatory compliance and device distribution, as it operates within the FDA’s jurisdiction.
Which regulatory registries list implantcast GmbH’s devices?
implantcast GmbH’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance with regulatory requirements.
How are implantcast GmbH’s devices classified under FDA regulations?
implantcast GmbH’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards due to moderate risk. The classification depends on factors like the device’s purpose, intended use, and potential risks, as outlined in FDA guidelines.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 324369826
Catalogue (1870)
Page 8 of 38| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| implacross® E PE insert 15° 4mm offset | 02483644 | FDA UDI | Class II | Active |
| EcoFit® | 30321625 | FDA UDI | Class II | Active |
| PE – cup insert 0° | 02803439 | FDA UDI | Class II | Active |
| Acs® | 42455310 | FDA UDI | Class II | Active |
| Acs® | 42005313 | FDA UDI | Class II | Active |
| MUTARS® engineers wrench SW 24 | 74900000 | FDA UDI | Class I | Active |
| Acs® | 42452611 | FDA UDI | Class II | Active |
| Acs® | 42019206 | FDA UDI | Class I | Active |
| Acs® | 42150469 | FDA UDI | Class II | Active |
| Actinia® | 80040720 | FDA UDI | Class II | Active |
| PE insert 10° 4mm offset | 02823252 | FDA UDI | Class II | Active |
| Acs® | 42150424 | FDA UDI | Class I | Active |
| MUTARS® screw | 57921002 | FDA UDI | Class II | Active |
| Acs® | 42144213 | FDA UDI | Class I | Active |
| Uni FB tibial component LL/RM | 40100013 | FDA UDI | Class II | Active |
| ic-head CoCrMo taper 12/14 | 23873200 | FDA UDI | Class II | Active |
| AGILON® XO screw for glenosphere | 38034061 | FDA UDI | Class II | Active |
| EcoFit® trial cup | 02203068 | FDA UDI | Class II | Active |
| Acs® | 42452510 | FDA UDI | Class II | Active |
| MUTARS® femoral stem cementless | 57600518 | FDA UDI | Class II | Active |
| implaFit® reamer conical | 80083034 | FDA UDI | Class I | Active |
| spongiosa screw flat head | 02801040 | FDA UDI | Class II | Active |
| Uni FB PE-insert | 40100214 | FDA UDI | Class II | Active |
| Agilon® | 78010178 | FDA UDI | Class II | Active |
| AGILON® stem cementless | 38524014 | FDA UDI | Class II | Active |
| Acs® | 42453311 | FDA UDI | Class II | Active |
| ic-head Biolox®delta taper 12/14 | 25863615 | FDA UDI | Class II | Active |
| AGILON® XO inverse cap base | 38634000 | FDA UDI | Class II | Active |
| GIS® retractor narrow | 75120921 | FDA UDI | Class I | Active |
| ACS® Uni Reamer guide | 42160345 | FDA UDI | Class I | Active |
| AGILON® trial screw | 78210040 | FDA UDI | Class II | Active |
| Acs® | 42451612 | FDA UDI | Class II | Active |
| Acs® | 42453517 | FDA UDI | Class II | Active |
| femoral neck reamer AO small | 75120021 | FDA UDI | Class I | Active |
| PB Uni tibial trial component | 40120020 | FDA UDI | Class II | Active |
| Acs® | 42452420 | FDA UDI | Class II | Active |
| Acs® | 42155059 | FDA UDI | Class I | Active |
| Acs® | 42102519 | FDA UDI | Class I | Active |
| Acs® | 42204056 | FDA UDI | Class II | Active |
| Acs® | 42102504 | FDA UDI | Class I | Active |
| AGILON® resection guide anatomic | 78200578 | FDA UDI | Class I | Active |
| AGILON® metaphyseal component omarthrosis | 3821000300 | FDA UDI | Class II | Active |
| AGILON® stem cementless | 38518015 | FDA UDI | Class II | Active |
| Acs® | 42150060 | FDA UDI | Class I | Active |
| AGILON® metaphyseal component trauma incl. safety screw | 38210061 | FDA UDI | Class II | Active |
| AGILON® XO CTA cap | 38624714 | FDA UDI | Class II | Active |
| Acs® | 42141212 | FDA UDI | Class I | Active |
| Acs® | 42104300 | FDA UDI | Class II | Active |
| Acs® | 4207505900 | FDA UDI | Class II | Active |
| ACS® Uni punch for femoral stem | 42160505 | FDA UDI | Class I | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- implantcast GmbH Buxtehude Lower Saxony · DE FEI 3012523063