Keisei Medical Industrial Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Keisei Medical Industrial Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Keisei Medical Industrial Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Bethel, US.
Historical record: 4 cleared submissions from 1986 to 1986. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Keisei Medical Industrial Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Keisei Medical Industrial Co., Ltd.
4 devices
Cleared
Sep 02, 1986
KEISEI SURGICAL BLADES (STERILE & NON-STERILE)
General & Plastic Surgery
13d
Cleared
Sep 02, 1986
KEISEI HANDLES FOR SURGICAL BLADES
General & Plastic Surgery
13d
Cleared
Sep 02, 1986
KEISEI SCALPEL (STERILE AND NON-STERILE)
General & Plastic Surgery
13d
Cleared
Sep 02, 1986
KEISEI MICRO-BLADES (STERILE AND NON-STERILE)
General & Plastic Surgery
13d