Pilkington Barnes-Hind, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pilkington Barnes-Hind, Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Pilkington Barnes-Hind, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 4 cleared submissions from 1994 to 1996. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Pilkington Barnes-Hind, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pilkington Barnes-Hind, Ltd.
4 devices
Cleared
Oct 01, 1996
PRECISION UV (VASURFILCON A)
Ophthalmic
180d
Cleared
Jul 05, 1995
HYDROCURVE 3 TORIC, II, II 55% TORIC, II APHAKIC 55%, SOFT MATE II, CUSTOM...
Ophthalmic
51d
Cleared
Jan 24, 1995
PRECISION UV(TM) (VASURFICON A)
Ophthalmic
43d
Cleared
Oct 03, 1994
PRECISION UV(TM) (VASURFILCON A)
Ophthalmic
4d