Medical Device Manufacturer · US , Harrisonburg , VA

Accudent, Inc.

1 submissions · 1 cleared · Since 1987

Total

Cleared

Denied

Accudent, Inc. — FDA 510(k) Submissions

Accudent, Inc. has submitted 1 FDA 510(k) premarket notifications since 1987, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Probe, Periodontic . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

ACCUDENT ACCUPROBE

K870280 · EIX Probe, Periodontic · Dental

Jun 1987 132d

Accudent, Inc.

Accudent, Inc. — FDA 510(k) Submissions

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