Conical Ti Base abutments
K-Number: K243521 · 2025-05-01
ApplicantBioHorizons Implant Systems, Inc.
Decision Date2025-05-01
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Conical Ti Base abutments is a medical device manufactured by BioHorizons Implant Systems, Inc.. It received FDA 510(k) clearance on 2025-05-01 under approval number K243521. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Conical Ti Base abutments?
Conical Ti Base abutments is a medical device that received FDA 510(k) clearance on 2025-05-01. It is manufactured by BioHorizons Implant Systems, Inc.. The 510(k) number is K243521.
When was Conical Ti Base abutments approved by the FDA?
Conical Ti Base abutments received FDA 510(k) clearance on 2025-05-01, under approval number K243521.
What company makes Conical Ti Base abutments?
Conical Ti Base abutments is manufactured by BioHorizons Implant Systems, Inc..
What is the FDA product code for Conical Ti Base abutments?
The FDA product code for Conical Ti Base abutments is NHA.
Related Clinical Trials
Other Devices by BioHorizons Implant Systems, Inc.
Related Devices (Code: NHA)
K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd.
K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG
K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A.
K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd.
K161435Temporary Snap AbutmentNobel Biocare AB
K160786RODO Abutment SystemRodo Medical, Inc.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.