# Aspide Medical

- Location (FDA's records): Washington, DC
- FDA decisions: 4 (2007–2012): 4 510(k) clearances
- Product codes: FTL (4)
- Predicates its devices cite: 16 (4 its own); citations of its devices by later devices: 5 (4 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- W. L. Gore & Associates, Inc.: 2 (https://510kreport.com/company/w-l-gore-associates)
- Sofradim Production: 2 (https://510kreport.com/company/sofradim-production)
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)
- Davol Inc., Sub. C. R. Bard, Inc.: 2 (https://510kreport.com/company/davol-sub-c-r-bard)
- American Medical Systems, Inc.: 1 (https://510kreport.com/company/american-medical-systems)
- Promedon: 1 (https://510kreport.com/company/promedon)
- Tissue Science Laboratories, Plc: 1 (https://510kreport.com/company/tissue-science-laboratories)
- Mentor Corp.: 1 (https://510kreport.com/company/mentor)

## Firms that cite its devices most
- Biomerix Corporation: 1 (https://510kreport.com/company/biomerix)

## Its most-cited devices
- K061445: Surgimesh WN (2007), cited by 3
- K072974: Surgimesh XB (2008), cited by 2

## Recent decisions
- K120025: Surgimesh XB - Skirted (Jun 26, 2012)
- K092233: Surgimesh XD (Jun 25, 2010)
- K072974: Surgimesh XB (Aug 18, 2008)
- K061445: Surgimesh WN (Feb 1, 2007)

Source page: https://510kreport.com/company/aspide-medical