FDA applicant

Renaissance Technology, Inc.

Newtown, PA2 decisions1992–19990 recalls

FDA records 2 decisions for Renaissance Technology, Inc. (Newtown, PA) from 1992 to 1999: 2 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) 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 Renaissance Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Renaissance Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Renaissance”

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

Renaissance Medical, Inc. 4 Renaissance Pharmaceutical, Inc. 4 Renaissance Instruments, LLC 1

Renaissance Technology, 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 “Renaissance”