FDA applicant

Ronvig Instruments, Ltd.

Dk-8721 Daugaard, DK2 decisions1990–20000 recalls

FDA records 2 decisions for Ronvig Instruments, Ltd. (Dk-8721 Daugaard, DK) from 1990 to 2000: 2 510(k) clearances. Most are in product codes EJI (Syringe, Cartridge) and EGM (Injector, Jet, Mechanical-Powered). 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 Instruments, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ronvig Instruments, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Ronvig Instruments, Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Ronvig”