Aesthetech Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aesthetech Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Aesthetech Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aesthetech Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aesthetech Corp.
6 devices
Cleared
Nov 25, 1987
CREAT BRAND O-RISE GENERAL ASPIRATOR
General & Plastic Surgery
58d
Cleared
Sep 11, 1987
CREAT BRAND MALAR IMPLANT
General & Plastic Surgery
16d
Cleared
Sep 24, 1985
CREAT BRAND I/A PACK CREAT BRAND PHACO PACK
Ophthalmic
56d
Cleared
Nov 06, 1984
CREAT BRAND SKIN EXPANDER
General & Plastic Surgery
49d
Cleared
Apr 24, 1984
DISPOSABLE SUCTION TUBING SET
General & Plastic Surgery
27d
Cleared
Sep 11, 1981
CREAT BRAND WAGNER CHIN IMPLANT
General & Plastic Surgery
38d