FDA applicant

Mountain Precision Mfg. Ltd. Co.

Boise, ID1 decision1994–19940 recalls

FDA records 1 decision for Mountain Precision Mfg. Ltd. Co. (Boise, ID) in 1994: 1 510(k) clearance. All are in product code ESE (Larynx, Artificial (Battery-Powered)). 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, ear, nose and throat panel, where it files most

How often FDA has decided Mountain Precision Mfg. Ltd. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mountain Precision Mfg. Ltd. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mountain Precision Mfg. Ltd. Co.’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 “Mountain”

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

Mountain Medical Equipment, Inc. 20 Mountain Shades, Inc. 3 Mountain Medico, Inc. 2 Mountain View Medical 2

Mountain Precision Mfg. Ltd. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mountain”