FDA applicant

The Center For Craniofacial & Dental Sleep Medicine

Sugarland, TX1 decision2017–20170 recalls

FDA records 1 decision for The Center For Craniofacial & Dental Sleep Medicine (Sugarland, TX) in 2017: 1 510(k) clearance. All are in product code LRK (Device, Anti-Snoring). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 The Center For Craniofacial & Dental Sleep Medicine’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — The Center For Craniofacial & Dental Sleep Medicine by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Center For Craniofacial & Dental…’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 “The”

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

Center Laboratories, Inc. 2 Center For Biomaterials and Advanced Technologies 1 Center For Marketing Services 1 Center For Orthotic and Prosthetic Care,Llc 1 Center For Disease Control and Prevention (Cdc) 1

The Center For Craniofacial & Dental Sleep Medicine

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “The”