FDA applicant

Kasios

Round Rock, TX1 decision2009–20090 recalls

FDA records 1 decision for Kasios (Round Rock, TX) in 2009: 1 510(k) clearance. All are in product code MQV (Filler, Bone Void, Calcium Compound). 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 Kasios’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Kasios by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Kasios”

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

Kasios Biomaterials 1

Kasios

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kasios”