FDA applicant

Invent Ent. (U.S.A.) Corp.

Hazlet, NJ1 decision1989–19890 recalls

FDA records 1 decision for Invent Ent. (U.S.A.) Corp. (Hazlet, NJ) in 1989: 1 510(k) clearance. All are in product code LYY (Latex Patient Examination Glove). 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, general hospital panel, where it files most

How often FDA has decided Invent Ent. (U.S.A.) Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Invent Ent. (U.S.A.) Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Invent Ent. (U.S.A.) Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Invent”

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

Invent Medical USA, LLC 3 Invent Medical Corporation 1

Invent Ent. (U.S.A.) Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Invent”