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Open, Classified

Osstem Dental X-Ray System T2Plus. Product Model Numbers T2-C-P and T2-CS-P.

FDA Recall Z-0315-2026 · Posted 2025-11-05

Recall StatusOpen, Classified
Product CodeOAS
Date Initiated2025-08-26

Reason for Recall

Osstem Implant Co. Ltd, is voluntarily initiating a medical device correction involving the current labeling for this electronic product may be missing a required Certification Statement under 21 CFR Subchapter J (Radiological Health Regulations). Specifically, the following statement may have been omitted: Certification Statement: This electronic product complies with all applicable performance standards prescribed under 21 CFR Subchapter J, as enforced by the U.S. Food and Drug Administration at the date of manufacturing.

Firm Action

Osstem Implant issued notification to customers, titled "URGENT: MEDICAL DEVICE CORRECTION", dated 08/26/2025, provided reason for recall, product description with UDI codes, corrective action, product disposition and contact information.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

U.S.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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