FDA applicant

Bredent-Products For the Dental Technician Laborat

Tuttlingen, DE3 decisions2005–20050 recalls

FDA records 3 decisions for Bredent-Products For the Dental Technician Laborat (Tuttlingen, DE) in 2005: 3 510(k) clearances. Most are in product codes EBG (Crown And Bridge, Temporary, Resin) and EBF (Material, Tooth Shade, Resin). Its devices cite 3 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 Bredent-Products For the Dental Technician Laborat’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bredent-Products For the Dental Technician Laborat since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bredent-Products For the Dental Technician Laborat by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bredent-Products For the Dental…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Bredent-Products”

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

Bredent GmbH & Co. KG 3

Bredent-Products For the Dental Technician Laborat

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Bredent-Products”