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Hiossen, Inc.

FDA 510(k) & PMA Approved Devices — 16 products

Total Devices16
Categories4
Latest FDA decision2026-05-14
TypeNumberDevice NameCodeDateActions
510(k) K253372 ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing AbutmentsNHA2026-05-14 View
510(k) K251427 EK MULTI ANGLED 30 ABUTMENTNHA2026-01-29 View
510(k) K241003 HIOSSEN Pre-milled Abutment (ET Pre-milled Abutment & EK Pre-milled Abutment)NHA2025-01-08 View
510(k) K240232 EK D3.3 and Ultra Wide ImplantsDZE2024-09-13 View
510(k) K233389 EK Digital AbutmentsNHA2024-05-29 View
510(k) K222636 ET Abutment SystemNHA2023-04-28 View
510(k) K203360 EK Implants and Abutments SystemDZE2022-01-07 View
510(k) K191751 EM ProvisionalDZE2019-12-16 View
510(k) K191201 EM SA Implant SystemDZE2019-11-15 View
510(k) K183242 ET IV SA Dental ImplantsDZE2019-05-21 View
510(k) K180527 IS3EKX2018-05-16 View
510(k) K170421 ET Hybrid AbutmentNHA2018-01-11 View
510(k) K162390 ET Hybrid AbutmentNHA2017-01-30 View
510(k) K153332 ETIII SA Fixture System (O3.2mm)DZE2016-10-27 View
510(k) K151542 A-OssNPM2016-08-03 View
510(k) K151626 ET III Bio-SA Fixture SystemDZE2016-07-21 View
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