Recall
FDAHealthAugust 26, 2025

OSSTEM Implant Co., Ltd. — Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS.

⚠️ 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.

Is this relevant to me?

Geography
Unknown
Source agency
FDA
Category
Health
Published
August 26, 2025

U.S.

What's affected?

Product
Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS.
Lot code
UDI Codes: 08800000995793 and 08800000995526.

Additional details

UDI Codes: 08800000995793 and 08800000995526.

What should I do?

Recommended action

Class II recall. FDA Mandated Quantity affected: N/A.

View original FDA notice →

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