FDA applicant

Princeton Regulatory Assoc.

Princeton, NJ4 decisions1996–19980 recalls

FDA records 4 decisions for Princeton Regulatory Assoc. (Princeton, NJ) from 1996 to 1998: 4 510(k) clearances. Most are in product codes KPN (Alarm, Conditioned Response Enuresis) and LHC (Warmer, Irrigation Solution). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Princeton Regulatory Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Princeton Regulatory Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Princeton Regulatory Assoc.’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 “Princeton”

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

Princeton BioMeditech Corp. 72 Princeton Biomedix 14 Princeton Applied Research Corp. 2 Princeton Medical Instruments, Inc. 2 Princeton Electronic Systems, Inc. 1

Princeton Regulatory Assoc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Princeton”