FDA applicant

Unique Management Ent., Inc.

Albany, NY2 decisions1995–19960 recalls

FDA records 2 decisions for Unique Management Ent., Inc. (Albany, NY) from 1995 to 1996: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). 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 Unique Management Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Unique Management Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Unique Management Ent., 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 “Unique”

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

Unique Flotation Systems, Inc. 2 Unique Optic, Ltd. 1 Unique Industries, Inc. 1 Unique Functional Products 1 Unique Hearing Technology, Inc. 1 Unique Bathing Supplies, Inc. 1

Unique Management Ent., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Unique”