# Surgical Instrument Service and Savings Inc.(Dba Medline Ren

- Location (FDA's records): Redmond, OR
- FDA decisions: 6 (2016–2024): 6 510(k) clearances
- Product codes: NUJ (2), NLQ (2), NLH (2)
- 510(k) review time since 2016: median 125 days, against 133 for FDA's reviews in the same codes and years (2 of 5 faster)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 13 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biosense Webster, Inc.: 2 (https://510kreport.com/company/biosense-webster)
- Covidien, Formerly Valleylab, A Division of Tyco H: 1 (https://510kreport.com/company/covidien-formerly-valleylab-a-division-of-tyco-h)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- Covidien, Formerly Valleylab, A Division of Tyco: 1 (https://510kreport.com/company/covidien-formerly-valleylab-a-division-of-tyco)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

## Recent decisions
- K241224: Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Auto ID Technology (BD710DF282CT, BD710DF282RTS, BD710FJ282RTS, BD710FJ282CT) (Nov 15, 2024)
- K193563: Medline ReNewal Reprocessed Harmonic ACE+7 Shears (Aug 19, 2020)
- K182588: Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/Divider (Oct 31, 2018)
- K170955: Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector (Jul 3, 2017)
- K153745: Medline ReNewal Reprocessed LigaSure Impact Open Sealer/Divider (May 2, 2016)
- K151617: Livewire Electrophysiology Catheter (Jan 22, 2016)

Source page: https://510kreport.com/company/surgical-instrument-service-and-savings-dba-medline-ren