Z-0315-2026 Class II Ongoing

Recalled by OSSTEM Implant Co., Ltd. — Haeundae District, N/A

Recall Details

Product Type
Devices
Report Date
November 12, 2025
Initiation Date
August 26, 2025
Termination Date
N/A
Voluntary/Mandated
FDA Mandated
Product Quantity
N/A

Product Description

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

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.

Distribution Pattern

U.S.

Code Information

UDI Codes: 08800000996059 and 08800000996042.