510(k) Report

FDA applicant

Mti Corp./ Electrostar S.A.-Haiti

Safety Harbor, FL1 decision1998–19980 recalls

FDA records 1 decision for Mti Corp./ Electrostar S.A.-Haiti (Safety Harbor, FL) in 1998: 1 510(k) clearance. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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, general and plastic surgery panel, where it files most

How often FDA has decided Mti Corp./ Electrostar S.A.-Haiti’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mti Corp./ Electrostar S.A.-Haiti since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mti Corp./ Electrostar S.A.-Haiti by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mti Corp./ Electrostar S.A.-Haiti’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?

  • GEIElectrosurgical, Cutting & Coagulation & Accessories1decision

What has FDA decided for it lately?

  • K974170DuostarMti Corp./ Electrostar S.A.-Haiti · 1998

The one decision as Mti Corp./ Electrostar S.A.-Haiti →