FDA applicant

Dyna-Pace Systems, Inc.

Atlanta, GA1 decision1992–19920 recalls

FDA records 1 decision for Dyna-Pace Systems, Inc. (Atlanta, GA) in 1992: 1 510(k) clearance. All are in product code EKJ (Burnisher, Operative). 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-Pace Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dyna-Pace Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dyna-Pace Systems, Inc. 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-Pace”

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 Dental Engineering BV 1

Dyna-Pace Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dyna-Pace”