Firstkind, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Firstkind, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: geko T-2 and geko Plus R-2
1
Total
1
Cleared
0
Denied
Firstkind, Ltd. has 1 FDA 510(k) cleared medical devices. Based in High Wycombe, GB.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Firstkind, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Firstkind, Ltd.
1 devices