510(k) Report

FDA applicant

Surgical Instrument Service and Savings (Dba Medline Renewal

Redmond, OR2 decisions2015–20160 recalls

FDA records 2 decisions for Surgical Instrument Service and Savings (Dba Medline Renewal (Redmond, OR) from 2015 to 2016: 2 510(k) clearances. Most are in product codes JOW (Sleeve, Limb, Compressible) and NLM (Laparoscope, General & Plastic Surgery…). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Surgical Instrument Service and Savings (Dba Medline Renewal’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2015: 12016: 1
2015high 1 (2015) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Surgical Instrument Service and Savings (Dba Medline Renewal by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • JOWSleeve, Limb, Compressible1decision
  • NLMLaparoscope, General & Plastic Surgery, Reprocessed1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K153258Medline ReNewal Reprocessed Versaport V2 Bladeless Optical TrocarsSurgical Instrument Service and Savings (Dba Medline Renewal · 2016
  • K143166Medline ReNewal Reprocessed Compression Limb SleevesSurgical Instrument Service and Savings (Dba Medline Renewal · 2015

All 2 as Surgical Instrument Service and Savings (Dba Medline Renewal →