Ormed Mfg., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ormed Mfg., Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Ormed Mfg., Inc. has 23 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 23 cleared submissions from 1983 to 1994.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ormed Mfg., Inc.
23 devices
Cleared
Jan 31, 1994
ARTROMOT K2 CPM
Physical Medicine
307d
Cleared
Jul 18, 1988
GAUZE SPONGE
General & Plastic Surgery
27d
Cleared
Jul 18, 1988
CYLINDRICAL SPONGE
General & Plastic Surgery
27d
Cleared
Jul 18, 1988
BUTCHER STRUNG TONSIL SPONGE
General & Plastic Surgery
27d
Cleared
Jul 18, 1988
TAPE STRUNG TONSIL SPONGE
General & Plastic Surgery
27d
Cleared
Mar 17, 1988
FLAT STICK SPONGE
General & Plastic Surgery
16d
Cleared
Mar 17, 1988
ROSEBUD DISSECTORS
General & Plastic Surgery
16d
Cleared
Mar 17, 1988
CHERRY SPONGE
General & Plastic Surgery
16d
Cleared
Mar 17, 1988
STRUNG ABSORBENT BALLS
General & Plastic Surgery
16d
Cleared
Mar 17, 1988
TRIANGLE SPONGE
General & Plastic Surgery
14d
Cleared
Mar 17, 1988
TRACHEOTOMY SPONGES
General & Plastic Surgery
14d
Cleared
Mar 17, 1988
ROUND STICK SPONGES
General & Plastic Surgery
14d