FDA applicant

Grantadler Corporation

Appollo Beach, FL2 decisions2008–20080 recalls

FDA records 2 decisions for Grantadler Corporation (Appollo Beach, FL) in 2008: 2 510(k) clearances. All are in product code LJT (Port & Catheter, Implanted, Subcutaneous…). Its devices cite 3 predicates, 0 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 hospital panel, where it files most

How often FDA has decided Grantadler Corporation’s devices, and how often a recall has named them.

FDA decisions per year

2in 2008

2008high 2 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Grantadler Corporation by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Grantadler”

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

Grantadler Corportation 1

Grantadler Corporation

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Grantadler”