Medical Device Manufacturer · US , Paso Robles , CA

Allied Biomedical Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1995

Recent clearances: KELOCATE SHEETING, DURALASTIC ANATOMICAL CHIN IMPLANTS, DURALASTIC ANATOMICAL MALAR IMPLANTS

9
Total
9
Cleared
0
Denied

FDA 510(k) Regulatory Record - Allied Biomedical Corp. General & Plastic Surgery ✕

9 devices
1-9 of 9
Cleared Aug 05, 1998
KELOCATE SHEETING
K982051 · MDA
General & Plastic Surgery · 55d
Cleared Jul 18, 1997
DURALASTIC ANATOMICAL CHIN IMPLANTS
K971478 · FWP
General & Plastic Surgery · 86d
Cleared Jul 18, 1997
DURALASTIC ANATOMICAL MALAR IMPLANTS
K971479 · LZK
General & Plastic Surgery · 86d
Cleared Jul 18, 1997
DURALASTIC ANATOMICAL NASAL IMPLANTS
K971481 · FZE
General & Plastic Surgery · 86d
Cleared May 28, 1997
DURALASTIC I AND DURALASTIC II
K971480 · MIB
General & Plastic Surgery · 35d
Cleared Feb 08, 1996
DURALASTIC I
K955368 · MIB
General & Plastic Surgery · 78d
Cleared Feb 08, 1996
DURALASTIC II
K955370 · MIB
General & Plastic Surgery · 78d
Cleared Jan 26, 1996
DURALASTIC SILICONE TUBING
K955433 · KGZ
General & Plastic Surgery · 59d
Cleared Nov 29, 1995
KELOCOTE
K954413 · MDA
General & Plastic Surgery · 69d
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