FDA applicant

Steri-Oss, Inc.

Yorba Linda, CA46 decisions1992–19981 recall

FDA records 46 decisions for Steri-Oss, Inc. (Yorba Linda, CA) from 1992 to 1998: 46 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and EMA (Cement, Dental). Its devices cite 6 predicates, 5 of them its own earlier devices. 1 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, dental panel, where it files most

How often FDA has decided Steri-Oss, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Steri-Oss, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Steri-Oss, 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 “Steri-Oss”

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

Steri-Shield Products, Inc. 5 Steri-Sytems, Corp. 1 Steri-Sol, Inc. 1 Steri-Aid, Inc. 1

Steri-Oss, 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?

What has been recalled?

Other applicant names beginning “Steri-Oss”