# Allied Biomedical Corp.

- Location (FDA's records): Paso Robles, CA
- FDA decisions: 9 (1995–1998): 9 510(k) clearances
- Product codes: MIB (3), MDA (2), LZK (1), FZE (1), KGZ (1), FWP (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Spirit Ridge Technologies: 2 (https://510kreport.com/company/spirit-ridge-technologies)

## Firms that cite its devices most
- Hanson Medical, Inc.: 3 (https://510kreport.com/company/hanson-medical)
- Boston Medical Products, Inc.: 3 (https://510kreport.com/company/boston-medical-products)
- Nagor, Ltd.: 1 (https://510kreport.com/company/nagor)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)

## Its most-cited devices
- K954413: Kelocote (1995), cited by 2
- K955370: Duralastic II (1996), cited by 1
- K971480: Duralastic I and Duralastic II (1997), cited by 1
- K971481: Duralastic Anatomical Nasal Implants (1997), cited by 1
- K955433: Duralastic Silicone Tubing (1996), cited by 1
- K971478: Duralastic Anatomical Chin Implants (1997), cited by 1

## Recent decisions
- K982051: Kelocate Sheeting (Aug 5, 1998)
- K971479: Duralastic Anatomical Malar Implants (Jul 18, 1997)
- K971481: Duralastic Anatomical Nasal Implants (Jul 18, 1997)
- K971478: Duralastic Anatomical Chin Implants (Jul 18, 1997)
- K971480: Duralastic I and Duralastic II (May 28, 1997)
- K955370: Duralastic II (Feb 8, 1996)
- K955368: Duralastic I (Feb 8, 1996)
- K955433: Duralastic Silicone Tubing (Jan 26, 1996)

Source page: https://510kreport.com/company/allied-biomedical