FDA applicant

Moss Tubes, Inc.

Elizabeth, NJ5 decisions1999–20190 recalls

FDA records 5 decisions for Moss Tubes, Inc. (Elizabeth, NJ) from 1999 to 2019: 5 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and BSS (Tube, Nasogastric). Its devices cite 2 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, gastroenterology and urology panel, where it files most

How often FDA has decided Moss Tubes, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2007high 1 (2019) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Moss Tubes, 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 “Moss”

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

Moss Medical Products 8 Moss Point Glove Co. 1 Moss Rehabilation Hospital 1

Moss Tubes, 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 “Moss”