FDA applicant

Straub Clinic and Hospital

Honolulu, HI2 decisions1987–19880 recalls

FDA records 2 decisions for Straub Clinic and Hospital (Honolulu, HI) from 1987 to 1988: 2 510(k) clearances. All are in product code KTT (Appliance, Fixation, Nail/Blade/Plate…). 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 Straub Clinic and Hospital’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Straub Clinic and Hospital since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Straub Clinic and Hospital by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Straub”

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

Straub Medical AG 1

Straub Clinic and Hospital

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Straub”