FDA applicant

Invamed Technologies, Inc.

Littleton, CO1 decision2004–20040 recalls

FDA records 1 decision for Invamed Technologies, Inc. (Littleton, CO) in 2004: 1 510(k) clearance. All are in product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). Its devices cite 3 predicates, 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Invamed Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Invamed 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 “Invamed”

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

Invamed, Inc. 1

Invamed Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Invamed”