# Via Surgical, Ltd.

- Location (FDA's records): Amirim, IL
- FDA decisions: 4 (2014–2021): 4 510(k) clearances
- Product codes: GDW (4)
- 510(k) review time since 2016: median 96 days, against 205 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 4 (4 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
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K132698: Fastouch Fixation System (2014), cited by 2
- K162252: FasTouch Fixation System (2016), cited by 1
- K181668: FasTouch Absorbable Fixation System (2019), cited by 1

## Recent decisions
- K203117: TissueTak device (Jan 7, 2021)
- K181668: FasTouch Absorbable Fixation System (Mar 13, 2019)
- K162252: FasTouch Fixation System (Nov 14, 2016)
- K132698: Fastouch Fixation System (Mar 14, 2014)

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