Aesthetic and Reconstructive Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aesthetic and Reconstructive Technologies, Inc. - FDA 510(k) Cleared ...
10
Total
10
Cleared
0
Denied
Aesthetic and Reconstructive Technologies, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Paso Robles, US.
Historical record: 10 cleared submissions from 2002 to 2003.
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 - Aesthetic and Reconstructive Technologies, Inc.
10 devices
Cleared
Jan 23, 2003
DIMISIL SCAR GEL
General & Plastic Surgery
83d
Cleared
Oct 10, 2002
AART SILICONE TUBING
General & Plastic Surgery
86d
Cleared
Aug 26, 2002
AART CALF IMPLANT
General & Plastic Surgery
27d
Cleared
Aug 08, 2002
AART SILICONE SHEETING
General & Plastic Surgery
30d
Cleared
Jul 16, 2002
AART SILICONE CARVING BLOCK
General & Plastic Surgery
42d
Cleared
Jul 16, 2002
AART GLUTEAL IMPLANT
General & Plastic Surgery
42d
Cleared
Jul 03, 2002
AART PECTORALIS IMPLANT
General & Plastic Surgery
68d
Cleared
Jul 02, 2002
AART CHIN IMPLANT
General & Plastic Surgery
60d
Cleared
Jul 02, 2002
AART NASAL IMPLANT
General & Plastic Surgery
60d
Cleared
Jul 02, 2002
AART MALAR IMPLANT
General & Plastic Surgery
60d