FDA applicant

Innovision Medical Technologies, LLC

Linthicum, MD1 decision2005–20050 recalls

FDA records 1 decision for Innovision Medical Technologies, LLC (Linthicum, MD) in 2005: 1 510(k) clearance. All are in product code MOD (Accessory To Continuous Ventilator (Respirator)). 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, anesthesiology panel, where it files most

How often FDA has decided Innovision Medical Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innovision Medical Technologies, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Innovision”

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

Innovision, Inc. 6 Innovision A/S 4 Innovision Medical, Inc. 2

Innovision Medical Technologies, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Innovision”