FDA applicant

Juniper Medical, Inc.

Pleasanton, CA2 decisions2007–20070 recalls

FDA records 2 decisions for Juniper Medical, Inc. (Pleasanton, CA) in 2007: 2 510(k) clearances. Most are in product codes ILO (Pack, Hot Or Cold, Water Circulating) and GEX (Powered Laser Surgical Instrument). Its devices cite 9 predicates, 1 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, physical medicine panel, where it files most

How often FDA has decided Juniper Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2007

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Juniper Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Juniper”

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

Juniper Medical Technology, Inc. 1

Juniper Medical, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Juniper”