FDA applicant

Wonder & Bioenergy Hi-Tech America, Inc.

Monterey Park, CA1 decision1999–19990 recalls

FDA records 1 decision for Wonder & Bioenergy Hi-Tech America, Inc. (Monterey Park, CA) in 1999: 1 510(k) clearance. All are in product code EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Wonder & Bioenergy Hi-Tech America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wonder & Bioenergy Hi-Tech America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wonder & Bioenergy Hi-Tech America, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wonder & Bioenergy Hi-Tech America, Inc.’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

Other applicant names beginning “Wonder”

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

Wonder Wire 2

Wonder & Bioenergy Hi-Tech America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Wonder”