# Salient Surgical Technologies, Inc.

- Location (FDA's records): Portsmouth, NH
- FDA decisions: 3 (2011–2011): 3 510(k) clearances
- Names in FDA's records: Salient Surgical Technologies, Inc. (2); Salient Surgical Technologies (1)
- Product codes: GEI (3)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 8 (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
- Tissuelink Medical, Inc.: 5 (https://510kreport.com/company/tissuelink-medical)
- Valleylab, Inc.: 2 (https://510kreport.com/company/valleylab)

## Firms that cite its devices most
- Medtronic Advanced Energy: 4 (https://510kreport.com/company/medtronic-advanced-energy)
- Medtronic, Inc.: 3 (https://510kreport.com/company/medtronic)
- Green Or, LLC: 1 (https://510kreport.com/company/green-or)

## Its most-cited devices
- K111285: Aquamantys 3 Pump Generator, Bipolar Sealer, Bipolar Sealer with Cutting (2011), cited by 3
- K111732: Aquamantys SBS 5.0 Sheated Biopolar Sealer (2011), cited by 3
- K101057: Aquamantys Double Cone Bipolar Sealer Model: 23-310-1 (2011), cited by 2

## Recent decisions
- K111732: Aquamantys SBS 5.0 Sheated Biopolar Sealer (Dec 5, 2011)
- K111285: Aquamantys 3 Pump Generator, Bipolar Sealer, Bipolar Sealer with Cutting (Sep 9, 2011)
- K101057: Aquamantys Double Cone Bipolar Sealer Model: 23-310-1 (Apr 5, 2011)

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