Atlas FDA

Hiossen Inc.

7 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Hiossen Inc.

RecordFirmDate
ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended for use with a dental implant to recall (Z-1271-2025)Hiossen Inc.2025-03-05
ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant t recall (Z-1272-2025)Hiossen Inc.2025-03-05
ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended for use with a dental implant t recall (Z-1273-2025)Hiossen Inc.2025-03-05
Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D 3.0G/H- Abutment is intended recall (Z-1274-2025)Hiossen Inc.2025-03-05
ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to recall (Z-1275-2025)Hiossen Inc.2025-03-05
Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is intended recall (Z-1276-2025)Hiossen Inc.2025-03-05
ET III Nano-HA fixture System ET NH Dental Implant Model # ET3R5010B -Intended for Dental recall (Z-1604-2023)Hiossen Inc.2023-05-18

Track Hiossen Inc. automatically

Every clearance here is in the API, with alerts when new ones post.