FDA applicant

Oculus Private Limited

Greenwood Village, CO2 decisions2011–20130 recalls

FDA records 2 decisions for Oculus Private Limited (Greenwood Village, CO) from 2011 to 2013: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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 Oculus Private Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Oculus Private Limited by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Oculus Private Limited’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 “Oculus”

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

Oculus Innovative Sciences 16 Oculus Optikgerate GmbH 8 Oculus America 1

Oculus Private Limited

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Oculus”