510(k) Report

FDA applicant

Medsol Corp.

New York, NY1 decision1998–19980 recalls

FDA records 1 decision for Medsol Corp. (New York, NY) in 1998: 1 510(k) clearance. All are in product code KNW (Instrument, Biopsy). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Medsol Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medsol Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medsol Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KNWInstrument, Biopsy1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K983187Medsol Goldenberg Bone Marrow Biopsy NeedleMedsol Corp. · 19982cite it

What has FDA decided for it lately?

  • K983187Medsol Goldenberg Bone Marrow Biopsy NeedleMedsol Corp. · 1998

The one decision as Medsol Corp. →