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Responsive Arthroscopy

Also registered as Responsive Arthroscopy, Inc., Responsive Arthroscopy, LLC

United Statesfrom the FDA registration address FDA establishment FEI 3015200759

Devices
13
Registrations
FDA
FDA recalls
0

Catalogue13

Newest first, rows 1-13 of 13

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Rows 1-13 of 13

Company details

FDA FEI number
3015200759
Address
701 N 3rd Street, Suite 208, Minneapolis, MN, 55401

Frequently asked questions

How many devices does RESPONSIVE ARTHROSCOPY have in the registry?

The registry currently lists 13 devices for RESPONSIVE ARTHROSCOPY. Devices recorded under merged duplicate company entries are counted once.

Which registries list RESPONSIVE ARTHROSCOPY's devices?

Among its 13 most recently registered devices, RESPONSIVE ARTHROSCOPY has devices listed in FDA 510(k) (13 devices).

What risk classes do RESPONSIVE ARTHROSCOPY's devices fall under?

Among its 13 most recently registered devices, the classes recorded for RESPONSIVE ARTHROSCOPY's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from RESPONSIVE ARTHROSCOPY in the registry?

The most recently registered devices listed for RESPONSIVE ARTHROSCOPY include Thunderbolt System, Responsive Arthroscopy Interference Screw System, Responsive Arthroscopy Wedge Push-In Suture Anchors and Mini Superhawk Suture Anchor System.

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.