FDA applicant

Propper Mfg. Co., Inc.

Long Island, NY25 decisions1977–20120 recalls

FDA records 25 decisions for Propper Mfg. Co., Inc. (Long Island, NY) from 1977 to 2012: 25 510(k) clearances. Most are in product codes JOJ (Indicator, Physical/Chemical Sterilization…) and FRC (Indicator, Biological Sterilization Process). Its devices cite 4 predicates, 2 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, general hospital panel, where it files most

How often FDA has decided Propper Mfg. Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Propper Mfg. Co., 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 “Propper”

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

Propper Manufacturing Co., Inc. 7

Propper Mfg. Co., 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 “Propper”