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Lincotek Medical LLC

Also registered as Lincotek Medical

United Statesfrom the FDA registration address FDA establishment FEI 3010039400

Devices
169
Registrations
FDA
FDA recalls
0

Catalogue169

Newest first, rows 1-50 of 169

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Rows 1-50 of 169

Showing 1-50 of 169

Company details

FDA FEI number
3010039400
Address
811 Northwoods Blvd, Vandalia, OH, 45377

Frequently asked questions

How many devices does Lincotek Medical LLC have in the registry?

The registry currently lists 169 devices for Lincotek Medical LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lincotek Medical LLC's devices?

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

What risk classes do Lincotek Medical LLC's devices fall under?

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

What are the newest devices from Lincotek Medical LLC in the registry?

The most recently registered devices listed for Lincotek Medical LLC include Integrity-SI Fusion System 1252-1012-076, Integrity-SI Fusion System 1252-1010-081, Integrity-SI Fusion System 1252-1012-106 and Integrity-SI Fusion System 1252-0006-030.

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.