# Haemoband Surgical, Ltd.

- Location (FDA's records): Belfast, GB
- FDA decisions: 2 (2009–2025): 2 510(k) clearances
- Product codes: FER (1), FHN (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (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
- Sapimed S.P.A.: 2 (https://510kreport.com/company/sapimed)
- Erchinger Medizintecnik: 1 (https://510kreport.com/company/erchinger-medizintecnik)

## Firms that cite its devices most
- Thd Spa: 1 (https://510kreport.com/company/thd)
- Inx Medical: 1 (https://510kreport.com/company/inx-medical)

## Its most-cited devices
- K091519: Haemoband Multi-Ligator (2009), cited by 2

## Recent decisions
- K250645: SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002) (Oct 9, 2025)
- K091519: Haemoband Multi-Ligator (Jul 28, 2009)

Source page: https://510kreport.com/company/haemoband-surgical