Medical Device Manufacturer · US , Walker , MI

Keller Instruments, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1983

Total

Cleared

Denied

Keller Instruments, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 5 cleared submissions from 1983 to 1985. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Keller Instruments, Inc. Filter by specialty or product code using the sidebar.

Keller Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Keller Instruments, Inc.

5 devices

1-5 of 5