FDA applicant

Eclipse Ventures

Princeton, NJ1 decision1996–19960 recalls

FDA records 1 decision for Eclipse Ventures (Princeton, NJ) in 1996: 1 510(k) clearance. All are in product code MMQ (Topographer, Corneal, Ac-Powered). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Eclipse Ventures since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Eclipse Ventures’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 “Eclipse”

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

Eclipse Medcorp, LLC 4 Eclipse Aesthetics, LLC 2 Eclipse Systems, Inc. 2 Eclipse, Inc. 1

Eclipse Ventures

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Eclipse”