Spectrum Designs, Inc.
Spectrum Designs, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1999.
Top product codes for Spectrum Designs, Inc.
Recent clearances by Spectrum Designs, Inc.
- K992522 — SPECTRUM DESIGNS SPECTRAGEL
- K982688 — SPECTRUM DESIGNS PRE-FORM CONTOUR SILICONE CARVING BLOCK
- K980444 — SPECTRUM DESIGNS BILATERAL GROOVE CHIN IMPLANT
- K980445 — SPECTRUM DESIGNS CONCAVE BACK CHIN IMPLANT
- K980446 — SPECTRUM DESIGNS ANTERIOR CHIN IMPLANT
- K980462 — SPECTRUM DESIGNS ANATOMICAL CHIN IMPLANT
- K980463 — SPECTRUM DESIGNS CURVILINEAR CHIN IMPLANT
- K980138 — SPECTRUM DESIGNS SYMMETRICAL CHIN IMPLANT
- K980461 — SPECTRUM DESIGNS CLEFT CHIN IMPLANT
- K980139 — SPECTRUM DESIGNS PROFILE MALAR IMPLANT
- K980140 — SPECTRUM DESIGNS MEDIAL MALAR IMPLANT
- K980141 — SPECTRUM DESIGNS PROJECTION MALAR IMPLANT
- K970702 — SPECTRUM DESIGNS SPECTRAGEL
- K960038 — SPECTRUM DESIGNS SILICONE BLOCK
- K944163 — SPECTRUM DISIGNS PECTORAL IMPLANT
- K944164 — MENISCUS CHIN IMPLANT
- K944165 — SILHOUETTE MALAR IMPLANT
- K944166 — DORSAL COLUMELLA IMPLANT
Data sourced from openFDA. This site is unofficial and independent of the FDA.