510(k) Report

FDA applicant

Intra Vantage, Inc.

Concord, CA1 decision1997–19970 recalls

FDA records 1 decision for Intra Vantage, Inc. (Concord, CA) in 1997: 1 510(k) clearance. All are in product code EGM (Injector, Jet, Mechanical-Powered). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Intra Vantage, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Intra Vantage, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EGMInjector, Jet, Mechanical-Powered1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K964802Cyberjet Local Anesthesia SystemIntra Vantage, Inc. · 19971cites it

What has FDA decided for it lately?

  • K964802Cyberjet Local Anesthesia SystemIntra Vantage, Inc. · 1997

The one decision as Intra Vantage, Inc. →

Other applicant names beginning “Intra”

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

Intra Luminal Therapeutics, Inc. 20Intra-Lock International 13Intra Lase Corp. 9Intra Special Catheters GmbH 1Intra-Sonix, Inc. 1Intra-Optics Labs. C/O Newman Assoc. 1