Medical Device Manufacturer · US , Houston , TX

Eye Garter Company, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1988

Total

Cleared

Denied

Eye Garter Company, Inc. has 6 FDA 510(k) cleared medical devices. Based in Houston, US.

Historical record: 6 cleared submissions from 1988 to 1990. Primary specialty: Ophthalmic.

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

Eye Garter Company, 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 - Eye Garter Company, Inc.

6 devices

1-6 of 6