FDA applicant

Dentsply Midwest

Des Plaines, IL1 decision1999–19990 recalls

FDA records 1 decision for Dentsply Midwest (Des Plaines, IL) in 1999: 1 510(k) clearance. All are in product code EJI (Syringe, Cartridge). Its devices cite 1 predicate, 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 Dentsply Midwest’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dentsply Midwest since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Dentsply”

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

Dentsply Intl. 291 Dentsply Sirona 88 Dentsply International, Inc. 59 Dentsply Interntional 13 Dentsply Implant 1 Dentsply Implants Manufacturing GmbH 1 Dentsply Ceramco 1 Dentsply Gendex 1

Dentsply Midwest

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Dentsply”