# Surgical Instrument Services and Savings, Inc.

- Location (FDA's records): Redmond, OR
- FDA decisions: 4 (2015–2023): 4 510(k) clearances
- Product codes: NUJ (2), NLQ (1), OWQ (1)
- 510(k) review time since 2016: median 151 days, against 78 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 3 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ethicon Endo-Surgery, Inc.: 2 (https://510kreport.com/company/ethicon-endo-surgery)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Irvine Biomedical, A St. Jude Medical Company: 1 (https://510kreport.com/company/irvine-biomedical-a-st-jude-medical)

## Recent decisions
- K232130: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter (Dec 15, 2023)
- K162751: Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider (May 1, 2017)
- K152313: Medline ReNewal Reprocessed Endopath Endoscopic Instruments (Jan 6, 2016)
- K150524: Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology (Dec 16, 2015)

Source page: https://510kreport.com/company/surgical-instrument-services-and-savings