510(k) Report

FDA applicant

Cmp Industries, LLC

Albany, NY7 decisions1990–20174 recalls

FDA records 7 decisions for Cmp Industries, LLC (Albany, NY) from 1990 to 2017: 7 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and EJH (Alloy, Metal, Base). Its devices cite 4 predicates, 1 of them its own earlier devices. 4 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Cmp Industries, LLC’s devices, and how often a recall has named them.

FDA decisions per year

2in 2017

2007: 12008: 12017: 2
2007high 2 (2017) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

3in 2016

2013: 12016: 3
2007high 3 (2016) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Cmp Industries, LLC’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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