FDA applicant

Craniofacial Pain Center of Idaho

Boise, ID1 decision2009–20090 recalls

FDA records 1 decision for Craniofacial Pain Center of Idaho (Boise, ID) in 2009: 1 510(k) clearance. All are in product code LRK (Device, Anti-Snoring). 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 Craniofacial Pain Center of Idaho’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Craniofacial Pain Center of Idaho by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Craniofacial Pain Center of Idaho’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 “Craniofacial”

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

Craniofacial Technologies, Inc. 1

Craniofacial Pain Center of Idaho

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Craniofacial”