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DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM

DIO Corporation · Model SSTI 6510N · UDI-DI 08800049281178

NHA Prescription
10
510(k) clearances
8,407
Adverse events (1 deaths)
225
Recalls
378
Facilities

Description

The DIO UF HSA Internal Sub-Merged Implant System is comprised of dental implants, Superstructures, Instruments for prosthetics and Surgical Instruments. The DIO UF HSA Internal Sub-Merged Implant System is specially designed for using in dental implant surery. A successfully osseointegrated implant willl achieve a firm implant when the fixture is operated under controlled conditions, per well known clinical studies. There are intended for use in partially or fully edendulous mandibles and maxillae, in support of single or multiple-unit restorations. The superstructures consist of screws(Cover Screw, Coping Screw), abutments(Screw retained type, Cemented retained type, Over denture retained type), Solid protect cap. The screws are made of commercial pure titanium, grade 4(ASTM F67) and Ti-6A1-4VELI(ASTM F136) intended to be used in a narrow tooth gap after implant insertion. And the screw is used to protect exposed top of the implant or to attach the abutment to implant.

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.