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Romd, LLC

United Statesfrom the FDA registration address FDA establishment FEI 3008959459

Devices
71
Registrations
FDA
FDA recalls
0

Catalogue71

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Company details

FDA FEI number
3008959459
Address
2967 Waterview Drive, Rochester Hills, MI, 48309

Frequently asked questions

How many devices does ROMD, LLC have in the registry?

The registry currently lists 71 devices for ROMD, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list ROMD, LLC's devices?

Among its 50 most recently registered devices, ROMD, LLC has devices listed in FDA GUDID (50 devices).

What risk classes do ROMD, LLC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for ROMD, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from ROMD, LLC in the registry?

The most recently registered devices listed for ROMD, LLC include Royal Oak Pedicle Screw System PS5.5-5.5-40, Royal Oak Pedicle Screw System PS5.5-4.5-40, Royal Oak Pedicle Screw System CCV5.5-43-50 and Royal Oak Pedicle Screw System 4301081.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.