510(k) Report

FDA applicant

Diamond Medical Equipment, Inc.

Jamaica, NY3 decisions1988–19910 recalls

FDA records 3 decisions for Diamond Medical Equipment, Inc. (Jamaica, NY) from 1988 to 1991: 3 510(k) clearances. Most are in product codes FNM (Mattress, Air Flotation, Alternating Pressure) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Diamond Medical Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diamond Medical Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Diamond Medical Equipment, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Diamond”

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