510(k) Report

FDA applicant

Illminoss Medical, Inc.

East Providence, RI1 decision2017–20170 recalls

FDA records 1 decision for Illminoss Medical, Inc. (East Providence, RI) in 2017: 1 De Novo grant. All are in product code QAD (Rod, Fixation, Intramedullary And Accessories…). 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, orthopedic panel, where it files most

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

FDA decisions per year

1in 2017

2017: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Illminoss Medical, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Illminoss Medical, Inc.’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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