510(k) Report

FDA applicant

Nobles Medical Technologies Ii, Inc.

Fountain Valley, CA3 decisions2012–20170 recalls

FDA records 3 decisions for Nobles Medical Technologies Ii, Inc. (Fountain Valley, CA) from 2012 to 2017: 3 510(k) clearances. All are in product code GAW (Suture, Nonabsorbable, Synthetic, Polypropylene). Its devices cite 1 predicate, 1 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 and plastic surgery panel, where it files most

How often FDA has decided Nobles Medical Technologies Ii, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2012: 22017: 1
2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Nobles Medical Technologies Ii, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nobles Medical Technologies Ii, 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 “Nobles”

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