Laxima Intl., Ltd. is one of 14 FDA 510(k) medical device manufacturers from Hong Kong in the dataset, ranked by real submission volume.
Laxima Intl., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Laxima Intl., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Central Hong Kong, HK.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Laxima Intl., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laxima Intl., Ltd.
1 devices