510(k) Report

FDA applicant

Mobile Dental Equipment Corp.

Bellevue, WA3 decisions1993–19930 recalls

FDA records 3 decisions for Mobile Dental Equipment Corp. (Bellevue, WA) in 1993: 3 510(k) clearances. Most are in product codes IZL (System, X-Ray, Mobile) and EIA (Unit, Operative Dental). 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 Mobile Dental Equipment Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mobile Dental Equipment Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mobile Dental Equipment Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • IZLSystem, X-Ray, Mobile1decision
  • EIAUnit, Operative Dental1decision
  • EHDUnit, X-Ray, Extraoral With Timer1decision

What has FDA decided for it lately?

  • K923354Port Opii, Port OpiiiMobile Dental Equipment Corp. · 1993
  • K923359Port-XPMobile Dental Equipment Corp. · 1993
  • K923360Port-XDMobile Dental Equipment Corp. · 1993

All 3 as Mobile Dental Equipment Corp. →

Other applicant names beginning “Mobile”

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

Mobile Care, Inc. 1