Jeff Klein Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jeff Klein Surgical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Jeff Klein Surgical, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Clemente, US.
Historical record: 5 cleared submissions from 1990 to 1990. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Jeff Klein Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jeff Klein Surgical, Inc.
5 devices
Cleared
May 24, 1990
KLEIN MICRO-CANNULA(TM)
General & Plastic Surgery
41d
Cleared
May 24, 1990
KLEIN LAMPREY-CANNULA(TM)
General & Plastic Surgery
41d
Cleared
May 22, 1990
KLEIN MICRO-CANNULA HANDLE(TM)
General & Plastic Surgery
39d
Cleared
May 11, 1990
KLEIN CORK(TM)
General & Plastic Surgery
28d
Cleared
May 11, 1990
KLEIN CONNECTOR(TM)
General & Plastic Surgery
28d