FDA applicant

Invivo Research Labs, Inc.

Mchenry, IL5 decisions1980–19870 recalls

FDA records 5 decisions for Invivo Research Labs, Inc. (Mchenry, IL) from 1980 to 1987: 5 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DSB (Plethysmograph, Impedance). 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 Labs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Invivo”

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

Invivo Corporation 39 Invivo Research, Inc. 14 Invivo Corporation (Business Trade Name: Philips) 6 Invivo Therapeutics Corporation 1

Invivo Research Labs, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Invivo”