FDA applicant

Innova Life Sciences Corp.

Washington, DC4 decisions2003–20060 recalls

FDA records 4 decisions for Innova Life Sciences Corp. (Washington, DC) from 2003 to 2006: 4 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and NHA (Abutment, Implant, Dental, Endosseous). Its devices cite 10 predicates, 3 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 Innova Life Sciences Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innova Life Sciences Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Innova Life Sciences 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

Other applicant names beginning “Innova”

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

Innova Vision, Inc. 11 Innova Corp. 6 Innova Spinal Technologies, LLC 2 Innova Vascular, Inc. 1

Innova Life Sciences Corp.

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 “Innova”