FDA applicant

Oasis

Glendora, CA2 decisions1995–20000 recalls

FDA records 2 decisions for Oasis (Glendora, CA) from 1995 to 2000: 2 510(k) clearances. Most are in product codes LYA (Splint, Intranasal Septal) and HNO (Keratome, Ac-Powered). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Oasis since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Oasis”

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

Oasis Medical, Inc. 17 Oasis Medikal Urunler Kimya Sanayi VE Tic A.S. 1 Oasis Research, LLC 1

Oasis

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Oasis”