FDA DeviceClass IINotable

FDA Recall: Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous De

Date: 2026-05-06
Brand: Straumann USA LLC
Category: Medical Device
FDA Class: Class II

Description

Includes an incorrect screw seat interface.

Hazard

Includes an incorrect screw seat interface.

Remedy

5 units

View original recall →
Share:

Related Recalls

2026-05-06 · FDA_DEVICE
FDA Recall: Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutmen
Straumann USA LLC
2026-04-01 · FDA_DEVICE
FDA Recall: Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
Straumann USA LLC
2026-04-01 · FDA_DEVICE
FDA Recall: Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;
Straumann USA LLC