FDA applicant

Lang Dental Manufacturing Co., Inc.

Wheeling, IL2 decisions2016–20170 recalls

FDA records 2 decisions for Lang Dental Manufacturing Co., Inc. (Wheeling, IL) from 2016 to 2017: 2 510(k) clearances. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Lang Dental Manufacturing Company, 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 Lang Dental Manufacturing Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2016high 1 (2016) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Lang Dental Manufacturing Co., Inc. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lang Dental Manufacturing Co., 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 “Lang”

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

Lang Dental Mfg. Co., Inc. 9

Lang Dental Manufacturing Co., Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Lang”