Hulaser, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Hulaser, Inc. - FDA 510(k) Cleared Devices
Recent clearances: K2 MOBILE
1
Total
1
Cleared
0
Denied
Hulaser, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hulaser, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hulaser, Inc.
1 devices