Stephens Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stephens Instruments - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Stephens Instruments has 5 FDA 510(k) cleared medical devices. Based in Lexington, US.
Historical record: 5 cleared submissions from 2002 to 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Stephens Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stephens Instruments
5 devices
Cleared
Nov 01, 2002
STEPHENS DISPOSABLE FORCEPS
Ophthalmic
66d
Cleared
Nov 01, 2002
STEPHENS DISPOSABLE SPECULUM
Ophthalmic
66d
Cleared
Nov 01, 2002
STEPHENS DISPOSABLE SCISSORS
Ophthalmic
66d
Cleared
Nov 01, 2002
STEPHENS DISPOSABLE HOOKS
Ophthalmic
66d
Cleared
Nov 01, 2002
GAYHEART CORNEAL EXCISION DEVICE
Ophthalmic
66d