FDA applicant

Lang Dental Mfg. Co., Inc.

Wheeling, IL9 decisions1994–20110 recalls

FDA records 9 decisions for Lang Dental Mfg. Co., Inc. (Wheeling, IL) from 1994 to 2011: 9 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and EBG (Crown And Bridge, Temporary, Resin). 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 Lang Dental Mfg. Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 3 (2008) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lang Dental Mfg. 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 Manufacturing Co., Inc. 2

Lang Dental Mfg. Co., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Lang”