FDA applicant

Ivivi Technologies, Inc.

Northvale, NJ1 decision2008–20080 recalls

FDA records 1 decision for Ivivi Technologies, Inc. (Northvale, NJ) in 2008: 1 510(k) clearance. All are in product code ILX (Diathermy, Shortwave, For Use Other Than…). 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, physical medicine panel, where it files most

How often FDA has decided Ivivi Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Ivivi Technologies, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Ivivi”

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

Ivivi Health Science, LLC 1

Ivivi Technologies, Inc.

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 “Ivivi”