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HomeSTERNGOLD DENTAL LLC › ERA® Implant Abutment Standard 0°, 4mm Cuff (M)

ERA® Implant Abutment Standard 0°, 4mm Cuff (M)

STERNGOLD DENTAL LLC · Model 811257 · UDI-DI 00841549101366

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

Description

ERA abutments provide a resilient attachment with universal hinge movement. Available as one piece straight abutment-screwed into implant and as a two-piece angled abutment (angled attachment cemented into abutment base, and base screed into 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.