FDA applicant

Invivo Therapeutics Corporation

Florida, FL1 decision2016–20160 recalls

FDA records 1 decision for Invivo Therapeutics Corporation (Florida, FL) in 2016: 1 510(k) clearance. All are in product code MOS (Coil, Magnetic Resonance, Specialty). 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, radiology panel, where it files most

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

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Invivo Therapeutics Corporation by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Invivo Therapeutics Corporation’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 Research Labs, Inc. 5

Invivo Therapeutics Corporation

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”