FDA applicant

Minimally Invasive Devices, LLC

Twinsburg, OH3 decisions2008–20150 recalls

FDA records 3 decisions for Minimally Invasive Devices, LLC (Twinsburg, OH) from 2008 to 2015: 3 510(k) clearances. Most are in product codes OCT (Anti Fog Solution And Accessories, Endoscopy) and GCJ (Laparoscope, General & Plastic Surgery). Its devices cite 5 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Minimally Invasive Devices, Inc.”.

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 Devices, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Minimally Invasive Devices, LLC by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Minimally”

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

Minimally Invasive Surgical Technologies, Inc. 6

Minimally Invasive Devices, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Minimally”