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SI

Shinhung MST Co., Ltd. · Model SIDAR5044H · UDI-DI 08809458310967

NHA Prescription
1
510(k) clearances
8,407
Adverse events (1 deaths)
225
Recalls
378
Facilities

Description

The Luna Dental Implant System is intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, and to restore the patient's chewing function. The Luna Dental Implant System is intended for delayed loading and immediate loading is possible when good primary stability is achieved and with appropriate occlusal loading.

Recalls

DateFirmReason
2026-07-13Straumann USA LLCThere may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the i
2026-03-27Straumann USA LLCIncludes an incorrect screw seat interface.
2026-03-27Straumann USA LLCIncludes an incorrect screw seat interface.
2026-03-17Straumann USA LLCA material mix-up had occurred during the manufacturing of Straumann Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorre
2026-03-17Straumann USA LLCA material mix-up had occurred during the manufacturing of Straumann Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorre
2025-09-30Prismatik Dentalcraft, Inc.Incorrect titanium screw, packaged with dental implant.
2025-06-25Preat CorpEngaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the
2025-06-24Preat CorpDue to manufacturing error, digital analog rotational feature is 180 degrees off.
2025-04-17Straumann USA LLCIncorrect blister labelling.
2025-04-02Preat CorpDue to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the ass

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.