Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Medentika CAD/CAM Abutments

K-Number: K242542 · 2025-04-22

ApplicantMedentika GmbH
Decision Date2025-04-22
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Medentika CAD/CAM Abutments is a medical device manufactured by Medentika GmbH. It received FDA 510(k) clearance on 2025-04-22 under approval number K242542. 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 Medentika CAD/CAM Abutments?

Medentika CAD/CAM Abutments is a medical device that received FDA 510(k) clearance on 2025-04-22. It is manufactured by Medentika GmbH. The 510(k) number is K242542.

When was Medentika CAD/CAM Abutments approved by the FDA?

Medentika CAD/CAM Abutments received FDA 510(k) clearance on 2025-04-22, under approval number K242542.

What company makes Medentika CAD/CAM Abutments?

Medentika CAD/CAM Abutments is manufactured by Medentika GmbH.

What is the FDA product code for Medentika CAD/CAM Abutments?

The FDA product code for Medentika CAD/CAM Abutments is NHA.

Other Devices by Medentika GmbH

K170838Medentika CAD/CAM TiBases K180564Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases K201711CARES Screw - Retained Bars and Bridges (SRBB) K200906MINICONE Implant K191123Multi-unit Abutments K223113Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments

View all 8 devices →

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.

↑