FDA applicant

Minimally Invasive Surgical Technologies, Inc.

Great Neck, NY6 decisions1993–19950 recalls

FDA records 6 decisions for Minimally Invasive Surgical Technologies, Inc. (Great Neck, NY) from 1993 to 1995: 6 510(k) clearances. All are in product code GCJ (Laparoscope, General & Plastic Surgery). 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 Minimally Invasive Surgical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Minimally Invasive Surgical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Minimally Invasive Surgical Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Minimally Invasive Surgical…’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 “Minimally”

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

Minimally Invasive Devices, LLC 3

Minimally Invasive Surgical Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Minimally”