FDA applicant

Ronvig A/S

Dk-8721 Daugaard, DK2 decisions2001–20030 recalls

FDA records 2 decisions for Ronvig A/S (Dk-8721 Daugaard, DK) from 2001 to 2003: 2 510(k) clearances. Most are in product codes KOJ (Airbrush) and EGS (Handpiece, Contra- And Right-Angle Attachment…). 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 Ronvig A/S’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ronvig A/S since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ronvig A/S by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Ronvig”

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

Ronvig Instruments, Ltd. 2 Ronvig Dental Mfg. A/S 1

Ronvig A/S

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ronvig”