Sinclair Pharmaceuticals, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Sinclair Pharmaceuticals, Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Sinclair Pharmaceuticals, Ltd. has 8 FDA 510(k) cleared medical devices. Based in Chinley, High Peak, GB.
Historical record: 8 cleared submissions from 2001 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sinclair Pharmaceuticals, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sinclair Pharmaceuticals, Ltd.
8 devices
Cleared
Oct 11, 2006
SINCLAIR SEBORRHEA EMULSION
General & Plastic Surgery
624d
Cleared
Jan 13, 2005
ALOCLAIR ORAL SPRAY
General & Plastic Surgery
104d
Cleared
Jun 21, 2004
ALOCLAIR ORAL GEL
General & Plastic Surgery
70d
Cleared
Sep 15, 2003
SALINUM, ORCLAIR
Dental
273d
Cleared
Jul 28, 2003
SINCLAIR WOUND AND SKIN EMULSION
General & Plastic Surgery
209d
Cleared
Dec 02, 2002
SST SALIVA SUPPORTING TABLETS
Pathology
81d
Cleared
Nov 25, 2002
ALOCLAIR ORAL RINSE
General & Plastic Surgery
63d
Cleared
Dec 21, 2001
GELCLAIR CONCENTRATED ORAL GEL
General & Plastic Surgery
101d