510(k) Report

FDA applicant

Surgical Instrument Services and Savings (Dba Medline Renewal

Redmond, OR1 decision2016–20160 recalls

FDA records 1 decision for Surgical Instrument Services and Savings (Dba Medline Renewal (Redmond, OR) in 2016: 1 510(k) clearance. All are in product code NLQ (Single-Use Reprocessed Ultrasonic Surgical…). Its devices cite 1 predicate, 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

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

FDA decisions per year

1in 2016

2016: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Surgical Instrument Services and Savings (Dba Medline… by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NLQSingle-Use Reprocessed Ultrasonic Surgical Instruments1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K151405Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue TechnologySurgical Instrument Services and Savings (Dba Medline Renewal · 2016

The one decision as Surgical Instrument Services and Savings (Dba Medline Renewal →