FDA applicant

Reliance Dental Mfg. Co.

Worth, IL2 decisions1985–19870 recalls

FDA records 2 decisions for Reliance Dental Mfg. Co. (Worth, IL) from 1985 to 1987: 2 510(k) clearances. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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, dental panel, where it files most

How often FDA has decided Reliance Dental Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reliance Dental Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Reliance”

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

Reliance Orthodontic Products, Inc. 32 Reliance Medical Systems, LLC 27 Reliance Medical Corp. 3 Reliance Industrial Co., Ltd. 1 Reliance Design & Manufacturing Corp. 1 Reliance Products Corp. 1 Reliance Medical Products, Inc. 1 Reliance Design & Manufacture Corp. 1

Reliance Dental Mfg. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Reliance”