510(k) Report

FDA applicant

Select Medical Systems, Inc.

Williston, VT6 decisions1995–20010 recalls

FDA records 6 decisions for Select Medical Systems, Inc. (Williston, VT) from 1995 to 2001: 6 510(k) clearances. Most are in product codes MFD (Cannula, Intrauterine Insemination) and HHK (Curette, Suction, Endometrial (And Accessories)). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Select Medical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Select Medical Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Select Medical Systems, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Select”

FDA records each applicant name separately; these may or may not be the same firm.