FDA applicant

Exelint Intl. Co.

Los Angeles, CA12 decisions2000–20100 recalls

FDA records 12 decisions for Exelint Intl. Co. (Los Angeles, CA) from 2000 to 2010: 12 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and MEG (Syringe, Antistick). 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 Exelint Intl. Co.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Exelint”

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

Exelint International, Co. 7

Exelint Intl. Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Exelint”