510(k) Report

FDA applicant

Comfort Acrylics Co.

Camas, WA3 decisions1990–20190 recalls

FDA records 3 decisions for Comfort Acrylics Co. (Camas, WA) from 1990 to 2019: 3 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and LRK (Device, Anti-Snoring). No recall is linked to its devices.

FDA’s records also spell it “Comfort Acrylics, Inc.”.

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 Comfort Acrylics Co.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Comfort Acrylics Co.’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 “Comfort”

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