Hydron , Ltd. is one of 279 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Hydron , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ACTIFRESH 400 LENS, ACTITORIC (OCUFILCON A) SOFT (HYDROPHILIC) TORIC CONTACT LENS FOR DAILY WEAR
2
Total
2
Cleared
0
Denied
Hydron , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Farnborough, Hants, GB.
Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Hydron , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hydron , Ltd.
2 devices