FDA applicant

Dyna Dental Engineering BV

2594 Ac Den Haag-Holland, NU1 decision1995–19950 recalls

FDA records 1 decision for Dyna Dental Engineering BV (2594 Ac Den Haag-Holland, NU) in 1995: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Dyna Dental Engineering BV’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dyna Dental Engineering BV since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dyna Dental Engineering BV by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Dyna”

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

Dyna Corp. 5 Dyna Flex 4 Dyna Flex, Intl. 4 Dyna-Med 4 Dyna-Tek Industries 2 Dyna Industries, Inc. 2 Dyna Care 1 Dyna-Pace Systems, Inc. 1

Dyna Dental Engineering BV

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dyna”