FDA applicant

Steiner Laboratories Div of Steiner Healthcare, LLC

Kapolei, HI1 decision2010–20100 recalls

FDA records 1 decision for Steiner Laboratories Div of Steiner Healthcare, LLC (Kapolei, HI) in 2010: 1 510(k) clearance. All are in product code LYC (Bone Grafting Material, Synthetic). 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, dental panel, where it files most

How often FDA has decided Steiner Laboratories Div of Steiner Healthcare, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Steiner Laboratories Div of Steiner Healthcare, LLC by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Steiner Laboratories Div of Steiner…’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 “Steiner”

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

Steiner Laboratories 4

Steiner Laboratories Div of Steiner Healthcare, LLC

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Steiner”