# Suturtek Incorporated

- Location (FDA's records): Acton, MA
- FDA decisions: 4 (2003–2008): 4 510(k) clearances
- Product codes: GAQ (3), GAL (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 3 (2 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
- Aesculap, Inc.: 2 (https://510kreport.com/company/aesculap)
- Qrc Consulting: 2 (https://510kreport.com/company/qrc-consulting)
- Cp Medical: 1 (https://510kreport.com/company/cp-medical)

## Firms that cite its devices most
- Sic Brevetti S.R.L.: 1 (https://510kreport.com/company/sic-brevetti)

## Its most-cited devices
- K063603: Suturtek Surgical Steel Suture, Models SC-S13, SC-S14, SC-S15, SC-S16, SC-S17 (2007), cited by 1
- K032468: Suturtek Fastclose Sternum Closure Device (2003), cited by 1
- K030227: Suturtek Fastclose Suturing Device (2003), cited by 1

## Recent decisions
- K082828: Suturtek 360 Degree Sternal Closure Device (Oct 14, 2008)
- K063603: Suturtek Surgical Steel Suture, Models SC-S13, SC-S14, SC-S15, SC-S16, SC-S17 (Feb 7, 2007)
- K032468: Suturtek Fastclose Sternum Closure Device (Sep 23, 2003)
- K030227: Suturtek Fastclose Suturing Device (Mar 17, 2003)

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