FDA applicant

Mini Lap Technologies, Inc.

Shelton, CT5 decisions2007–20100 recalls

FDA records 5 decisions for Mini Lap Technologies, Inc. (Shelton, CT) from 2007 to 2010: 5 510(k) clearances. Most are in product codes OCW (Endoscopic Tissue Approximation Device) and GCJ (Laparoscope, General & Plastic Surgery). Its devices cite 8 predicates, 2 of them its own earlier devices. 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 Mini Lap Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2010

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mini Lap Technologies, Inc.’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 “Mini”

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

Mini-Mitter Co., Inc. 5 Mini Floss 1

Mini Lap Technologies, Inc.

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 “Mini”