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Sign in to claim this brandMerete GmbH
US
Last updated May 24, 2026
What Merete GmbH makes
Merete GmbH manufactures orthopaedic fixation devices, including non-sliding bone screws (such as the MECRON™ Cannulated Screw and Merete® CS Cortical Screw), diaphysis and knee arthrodesis prostheses (e.g., OsteoBridge™), orthopaedic bone wires (e.g., K-Wires trocar tip round end), non-bioabsorbable fixation plates, implantable bone washers (e.g., MECRON™ Washer), reusable orthopaedic impactors, and single-use fluted surgical drill bits.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Merete GmbH 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 Merete GmbH manufacture?
Merete GmbH specializes in orthopaedic fixation devices. These include non-sliding bone screws like the MECRON™ Cannulated Screw and Merete® CS Cortical Screw, diaphysis and knee arthrodesis prostheses (such as OsteoBridge™), orthopaedic bone wires (e.g., K-Wires trocar tip round end), non-bioabsorbable fixation plates, implantable bone washers (e.g., MECRON™ Washer), reusable orthopaedic impactors, and single-use fluted surgical drill bits. These products are designed for bone stabilization and joint reconstruction.
Where is Merete GmbH based?
Merete GmbH is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
Which regulatory registries list Merete GmbH’s devices?
Merete GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for medical devices authorized in the U.S. The UDI system helps healthcare providers and regulators identify and verify specific devices.
How are Merete GmbH’s devices classified under FDA regulations?
Merete GmbH’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and often require general controls for regulation, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and clinical impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- merete-medical.com
- —
- —
- [email protected]
- Phone
- +1(630)869-1092
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 313267265
Catalogue (1535)
Page 25 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MECRON™ Cannulated Screw | 4.0 42 T10 short thread | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 4.0 50 T10 short thread | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Fully Threaded | 3.0 24 T10 | FDA UDI | Class II | Unknown |
| MetaFix™ LS Locking Screw | 3.8 40 T10 | FDA UDI | Class II | Unknown |
| DuoThread™ Scarf cannulated screw fully threaded | 3.0 10 | FDA UDI | Class II | Unknown |
| OsteoBridge™ IKA Knee Arthrodesis Nail | without Collar 16 150 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 2.0 42 T8 short thread | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Fully Threaded | 3.0 30 | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Fully Threaded | 3.5 36 T10 | FDA UDI | Class II | Unknown |
| MetaFix™ LS Locking Screw | 3.8 22 T10 | FDA UDI | Class II | Unknown |
| OsteoBridge™ IDSF Diaphysis Tibial Nail | 10 60 | FDA UDI | Class II | Active |
| K-Wires trocar tip round end | 2.00 150 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 2.0 22 T8 short thread | FDA UDI | Class II | Active |
| Merete® Cannulated HCS Headless Compression Screw | 6.5 110 Hex3.5 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 2.5 14 T8 full thread | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Partly Threaded | 3.5 32 | FDA UDI | Class II | Unknown |
| MetaToe™ EndoSorb™ Hammer Toe Pin | 2.7 22 | FDA UDI | Class II | Unknown |
| MetaFix™ LS Locking Screw | 3.5 24 Hex2.5 | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Partly Threaded | 3.5 38 T10 | FDA UDI | Class II | Unknown |
| MetaFix™ LS Locking Screw | 3.5 20 Hex2.5 | FDA UDI | Class II | Active |
| MetaFix™ LS Locking Screw | 3.8 48 T10 | FDA UDI | Class II | Active |
| Merete® Cannulated HCS Headless Compression Screw | 4.3 28 Hex2.5 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 3.0 34 T10 short thread | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 3.0 28 T10 full thread | FDA UDI | Class II | Active |
| MetaFix™ LS Locking Screw | 3.0 32 T10 | FDA UDI | Class II | Unknown |
| Merete® CS Cortical Screw Partly Threaded | 3.0 24 T10 | FDA UDI | Class II | Unknown |
| Merete® Cannulated HCS Headless Compression Screw | 4.3 48 Hex2.5 | FDA UDI | Class II | Active |
| Merete® Cannulated HCS Headless Compression Screw | 4.3 36 Hex2.5 | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Partly Threaded | 3.5 28 T10 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 4.0 12 T10 short thread | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 3.5 44 T10 full thread | FDA UDI | Class II | Active |
| OsteoBridge™ IDSF Diaphysis Tibial Nail | 10 70 | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Partly Threaded | 3.0 28 T10 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 3.5 34 T10 short thread | FDA UDI | Class II | Active |
| Merete® Cannulated PCS Compression Screw | 3.0 14 T10 | FDA UDI | Class II | Unknown |
| MetaFix™ LS Locking Screw | 3.8 20 Hex2.5 | FDA UDI | Class II | Unknown |
| OsteoBridge™ | GA31015 | FDA UDI | Class I | Active |
| MetaFix™ LS Locking Screw | 3.0 14 T10 | FDA UDI | Class II | Unknown |
| Merete® CS Cortical Screw Fully Threaded | 3.5 20 T10 | FDA UDI | Class II | Active |
| Merete® Cannulated HCS Headless Compression Screw | 3.0 12 Hex2.5 | FDA UDI | Class II | Active |
| OsteoBridge™ Interlocking Screw | 5.0 24 | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 3.5 22 T10 short thread | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 2.5 48 T8 short thread | FDA UDI | Class II | Active |
| Merete® CS Cortical Screw Fully Threaded | 3.0 28 T10 | FDA UDI | Class II | Unknown |
| OsteoBridge™ IDSF Diaphysis Reducing bushing | 7 for Spacer 20 | FDA UDI | Class II | Unknown |
| Merete® CS Cortical Screw Fully Threaded | 3.5 16 T10 | FDA UDI | Class II | Unknown |
| MECRON™ Cannulated Screw | 3.5 48 T10 short thread | FDA UDI | Class II | Active |
| MECRON™ Cannulated Screw | 2.5 40 T8 short thread | FDA UDI | Class II | Active |
| SCARFix™ Locking Plate | right 42 | FDA UDI | Class II | Unknown |
| MetaFix™ LS Locking Screw | 3.0 12 Hex2.5 | FDA UDI | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Merete Gmbh BERLIN · DE FEI 3002949614