FDA applicant

Noble Fiber Technologies, Inc.

Clarks Summit, PA8 decisions2004–20070 recalls

FDA records 8 decisions for Noble Fiber Technologies, Inc. (Clarks Summit, PA) from 2004 to 2007: 8 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and ISH (Component, External, Limb, Ankle/Foot). Its devices cite 31 predicates, 5 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Noble Fiber Technologies”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Noble Fiber Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Noble Fiber Technologies, 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 “Noble”

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

Noble Marketing 2 Noble Optic 1 Noble Anesthesia-Air, Inc. 1

Noble Fiber Technologies, 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 “Noble”