FDA applicant

Summa Intl.

Phoenix, AZ1 decision1989–19890 recalls

FDA records 1 decision for Summa Intl. (Phoenix, AZ) in 1989: 1 510(k) clearance. All are in product code LYY (Latex Patient Examination Glove). 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 Summa Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Summa Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Summa”

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

Summa Therapeutics, LLC 3 Summa Medical Corp. 1

Summa Intl.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Summa”