# G.W.B. Intl., Ltd.

- Location (FDA's records): Sudbury, MA
- FDA decisions: 8 (1990–1996): 8 510(k) clearances
- Product codes: OKS (3), LZU (3), HPZ (1), IYO (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Eagle Vision, Inc.: 1 (https://510kreport.com/company/eagle-vision)
- Fci (France Chirurgie Instrumentation) Sas: 1 (https://510kreport.com/company/fci-france-chirurgie-instrumentation)

## Its most-cited devices
- K955671: Ritleng Bican.Lacr.Sets/Self Thread. Monokas (CHG.in Ster.) (1996), cited by 2

## Recent decisions
- K955671: Ritleng Bican.Lacr.Sets/Self Thread. Monokas (CHG.in Ster.) (Mar 6, 1996)
- K954094: Ophta Sil- Punctal Plugs (Modification) (Oct 5, 1995)
- K950569: Ophta Sil {Self-Threading Monoka (Ritleng Type)} (Mar 14, 1995)
- K940508: Ophta Sil (Ritleng Probe and Lacrimal Intubation Set) (May 4, 1994)
- K911110: Ophta Sil (R), Enulceation/Evisceration Implants (Jun 18, 1991)
- K911108: Ophta Sil (R), Punctal Plugs and Inserters (May 13, 1991)
- K911109: Ophta Sil (R), Lachrymal Intubation Sets (May 1, 1991)
- K896029: Digital Ultrasound Imaging System Dub 20 (Jan 12, 1990)

Source page: https://510kreport.com/company/gwb-intl