Medical Device Manufacturer · US , San Marcos , CA

Blade Works, Inc.

3 submissions · 3 cleared · Since 1999
3
Total
3
Cleared
0
Denied

Blade Works, Inc. — FDA 510(k) Submissions

Blade Works, Inc. has submitted 3 FDA 510(k) premarket notifications since 1999, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Keratome, Ac-powered, Device, Irrigation, Ocular Surgery . Use the specialty filter in the sidebar to narrow results.

3 devices
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All3 Ophthalmic 3