Medical Device Manufacturer · US , Walker , MI

The Telos Co.

2 submissions · 2 cleared · Since 1981
2
Total
2
Cleared
0
Denied

The Telos Co. — FDA 510(k) Submissions

The Telos Co. has submitted 2 FDA 510(k) premarket notifications since 1981, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Goniometer, Nonpowered, Apparatus, Traction, Non-powered . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Neurology 1 Radiology 1