Cleared Traditional

K142118 - INCLUSIVE TITANIUM ABUTMENTS COMPATIBLE WITH: STRAUMANN BONE LEVEL, NOBEL BIOCARE BRANAE (FDA 510(k) Clearance)

Nov 2014
Decision
113d
Days
Class 2
Risk

K142118 is an FDA 510(k) clearance for the INCLUSIVE TITANIUM ABUTMENTS COMPATIBLE WITH: STRAUMANN BONE LEVEL, NOBEL BIOCARE BRANAE. This device is classified as a Abutment, Implant, Dental, Endosseous (Class II - Special Controls, product code NHA).

Submitted by Prismatik Dentalcraft, Inc. (Irvine, US). The FDA issued a Cleared decision on November 25, 2014, 113 days after receiving the submission on August 4, 2014.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3630. To Be Used In Conjunction With An Endosseous Dental Implant Fixture To Aid In Prosthetic Rehabilitation..

Submission Details

510(k) Number K142118 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 2014
Decision Date November 25, 2014
Days to Decision 113 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code NHA — Abutment, Implant, Dental, Endosseous
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3630
Definition To Be Used In Conjunction With An Endosseous Dental Implant Fixture To Aid In Prosthetic Rehabilitation.

Similar Devices — NHA Abutment, Implant, Dental, Endosseous

All 80
Healing Abutment System
K251434 · Osstem Implant Co., Ltd. · Mar 2026
EK MULTI ANGLED 30 ABUTMENT
K251427 · Hiossen, Inc. · Jan 2026
Straumann Variobase Abutments XC for Bridge/Bar
K253315 · Institut Straumann AG · Jan 2026
Atlantis® Abutments in Titanium
K252343 · Dentsply Sirona · Dec 2025
CEREC Tessera Abutment System
K252248 · Dentsply Sirona · Nov 2025
Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants
K251205 · Dentsply Sirona · Nov 2025