FDA applicant

Cefla Dental Group

North Attleboro, MA2 decisions2010–20100 recalls

FDA records 2 decisions for Cefla Dental Group (North Attleboro, MA) in 2010: 2 510(k) clearances. All are in product code MUH (System, X-Ray, Extraoral Source, Digital). Its devices cite 4 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 Cefla Dental Group’s devices, and how often a recall has named them.

FDA decisions per year

2in 2010

2010high 2 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Cefla Dental Group by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cefla Dental Group’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 “Cefla”

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

Cefla S.C. 21 Cefla S.C.R.L. 3 Cefla S.C. Cefla Dental Group 1

Cefla Dental Group

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Cefla”