Spectrum Designs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectrum Designs, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Spectrum Designs, Inc. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Goleta, US.
Historical record: 18 cleared submissions from 1994 to 1999.
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 - Spectrum Designs, Inc.
18 devices
Cleared
Oct 26, 1999
SPECTRUM DESIGNS SPECTRAGEL
General & Plastic Surgery
90d
Cleared
Oct 13, 1998
SPECTRUM DESIGNS PRE-FORM CONTOUR SILICONE CARVING BLOCK
General & Plastic Surgery
71d
Cleared
May 06, 1998
SPECTRUM DESIGNS BILATERAL GROOVE CHIN IMPLANT
General & Plastic Surgery
90d
Cleared
May 06, 1998
SPECTRUM DESIGNS CONCAVE BACK CHIN IMPLANT
General & Plastic Surgery
90d
Cleared
May 06, 1998
SPECTRUM DESIGNS ANTERIOR CHIN IMPLANT
General & Plastic Surgery
90d
Cleared
May 06, 1998
SPECTRUM DESIGNS ANATOMICAL CHIN IMPLANT
General & Plastic Surgery
90d
Cleared
May 06, 1998
SPECTRUM DESIGNS CURVILINEAR CHIN IMPLANT
General & Plastic Surgery
90d
Cleared
Apr 03, 1998
SPECTRUM DESIGNS SYMMETRICAL CHIN IMPLANT
General & Plastic Surgery
78d
Cleared
Mar 04, 1998
SPECTRUM DESIGNS CLEFT CHIN IMPLANT
General & Plastic Surgery
27d
Cleared
Mar 03, 1998
SPECTRUM DESIGNS PROFILE MALAR IMPLANT
General & Plastic Surgery
47d
Cleared
Mar 03, 1998
SPECTRUM DESIGNS MEDIAL MALAR IMPLANT
General & Plastic Surgery
47d
Cleared
Mar 03, 1998
SPECTRUM DESIGNS PROJECTION MALAR IMPLANT
General & Plastic Surgery
47d