FDA applicant

Invivo Research, Inc.

Orlando, FL14 decisions1989–20050 recalls

FDA records 14 decisions for Invivo Research, Inc. (Orlando, FL) from 1989 to 2005: 14 510(k) clearances. Most are in product codes MWI (Monitor, Physiological, Patient (Without…) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). Its devices cite 19 predicates, 5 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Invivo Research, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Invivo Research, 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 “Invivo”

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

Invivo Corporation 39 Invivo Corporation (Business Trade Name: Philips) 6 Invivo Research Labs, Inc. 5 Invivo Therapeutics Corporation 1

Invivo Research, 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 “Invivo”