FDA applicant

Peripheral Ave

Santa Rosa, CA2 decisions1998–19990 recalls

FDA records 2 decisions for Peripheral Ave (Santa Rosa, CA) from 1998 to 1999: 2 510(k) clearances. All are in product code FGE (Stents, Drains And Dilators For The Biliary…). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Peripheral Ave since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Peripheral”

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

Peripheral Systems Group 17

Peripheral Ave

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 “Peripheral”