510(k) Report

FDA applicant

Pop Medical Solutions

Tel Aviv, IL1 decision2016–20161 recall

FDA records 1 decision for Pop Medical Solutions (Tel Aviv, IL) in 2016: 1 510(k) clearance. All are in product code PBQ (Fixation, Non-Absorbable Or Absorbable, For…). Its devices cite 1 predicate, 0 of them its own earlier devices. 1 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Pop Medical Solutions’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

1in 2021

2021: 1
2016high 1 (2021) · low 0 (2016)2026

Class I Class II/III not classified

FIG. 1 — Pop Medical Solutions 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?

  • PBQFixation, Non-Absorbable Or Absorbable, For Pelvic Use1decision

Whose devices does it build on?

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

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K160569NeuGuidePop Medical Solutions · 20161cites it

What has FDA decided for it lately?

  • K160569NeuGuidePop Medical Solutions · 20161 recall

The one decision as Pop Medical Solutions →

What has been recalled?

1 recall linked to its devices; the latest:

  • K160569The EnPlace is a single use trans-vaginal pelvic floor repair system which enables…Dec 13, 2021Class II