Merete GmbH
GermanyFDA applicant, unverified FDA FEI 3002949614
- Devices
- 1,687
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
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.
Catalogue
Search and filter all 1,687 devicesShowing 1-50 of 1,687
Company details
- FDA FEI number
- 3002949614
- DUNS number
- 313267265
- Address
- 102 ALT LANKWITZ, BERLIN
- Phone
- +1(630)869-1092
Frequently asked questions
How many devices does Merete GmbH have in the registry?
The registry currently lists 1687 devices for Merete GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Merete GmbH's devices?
Among its 50 most recently registered devices, Merete GmbH has devices listed in FDA GUDID (50 devices).
What risk classes do Merete GmbH's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Merete GmbH's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Merete GmbH in the registry?
The most recently registered devices listed for Merete GmbH include DuoMetaCun™ II Plate 33 25, MultiCup™ HF40100, MECRON™ Cannulated Screw 3.5 22 T10 short thread and MetaFix™ LS Locking Screw 3.5 30 T10.