Kinetic Biomedical Services, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kinetic Biomedical Services, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Kinetic Biomedical Services, Inc. has 5 FDA 510(k) cleared medical devices. Based in Erie, US.
Historical record: 5 cleared submissions from 1989 to 1989. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kinetic Biomedical Services, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kinetic Biomedical Services, Inc.
5 devices
Cleared
Jun 15, 1989
KINETIC MODEL 700
General & Plastic Surgery
59d
Cleared
Apr 19, 1989
KINETIC MODEL 500
General & Plastic Surgery
27d
Cleared
Apr 19, 1989
KINETIC MODEL 1000
General & Plastic Surgery
27d
Cleared
Apr 19, 1989
KINETIC MODEL 132
General & Plastic Surgery
27d
Cleared
Apr 19, 1989
KINETIC MODEL 330
General & Plastic Surgery
27d