Medical Device Manufacturer · US , Oxford , MA

Acueity, Inc.

4 submissions · 4 cleared · Since 2001
4
Total
4
Cleared
0
Denied

Acueity, Inc. — FDA 510(k) Submissions

Acueity, Inc. has submitted 4 FDA 510(k) premarket notifications since 2001, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Light Source, Fiberoptic, Routine, Instrument, Biopsy, Light Source, Endoscope, Xenon Arc . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Gastroenterology & Urology 3 General & Plastic Surgery 1