# Sapimed S.P.A.

- Location (FDA's records): Crofton, MD
- FDA decisions: 3 (2007–2007): 3 510(k) clearances
- Product codes: FER (1), KDM (1), FHN (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Welch Allyn, Inc.: 2 (https://510kreport.com/company/welch-allyn)
- Canadian Theatre Products, Ltd.: 1 (https://510kreport.com/company/canadian-theatre-products)
- North Eos Industries, Inc.: 1 (https://510kreport.com/company/north-eos-industries)
- Patrick J. O'Regan: 1 (https://510kreport.com/company/patrick-j-o-regan)
- Erchinger Medizintecnik: 1 (https://510kreport.com/company/erchinger-medizintecnik)

## Firms that cite its devices most
- Thd Spa: 3 (https://510kreport.com/company/thd)
- Haemoband Surgical, Ltd.: 2 (https://510kreport.com/company/haemoband-surgical)
- Applied Medical Resources: 2 (https://510kreport.com/company/applied-medical-resources)
- Angiologica B. M. Srl: 1 (https://510kreport.com/company/angiologica-b-m)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)

## Its most-cited devices
- K070913: Self-Light Disposable Anoscope (2007), cited by 5
- K070915: Sapimed Disposable Sigmoidoscope (2007), cited by 2
- K070881: Lem Hemorrhoidal Ligator, Models a.5650, a.5660 (2007), cited by 2

## Recent decisions
- K070881: Lem Hemorrhoidal Ligator, Models a.5650, a.5660 (Sep 26, 2007)
- K070913: Self-Light Disposable Anoscope (Aug 10, 2007)
- K070915: Sapimed Disposable Sigmoidoscope (Jul 6, 2007)

Source page: https://510kreport.com/company/sapimed