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FDA 510(k)

Multi-Unit DAS System

K-Number: K231559 · 2023-11-17

ApplicantTalladium España, SL
Decision Date2023-11-17
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Multi-Unit DAS System is the device name listed in this FDA 510(k) record. The listed applicant is Talladium España, SL. It received FDA 510(k) clearance on 2023-11-17 under 510(k) number K231559. 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 Multi-Unit DAS System?

Multi-Unit DAS System is a medical device that received FDA 510(k) clearance on 2023-11-17. The listed applicant is Talladium España, SL. The 510(k) number is K231559.

When did Multi-Unit DAS System receive FDA 510(k) clearance?

Multi-Unit DAS System received FDA 510(k) clearance on 2023-11-17, under 510(k) number K231559.

Who is the listed applicant for Multi-Unit DAS System?

The FDA 510(k) record lists Talladium España, SL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi-Unit DAS System?

The FDA product code for Multi-Unit DAS System is NHA.

Other records listing Talladium España, SL as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243732Multi-Unit DAS SystemK243425Guided DAS Surgical KitK243530Dynamic TiBaseK241170Dynamic TiBase; TRI ScrewsK232151Dynamic TiBaseK212108Dynamic TiBase

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Related Devices (Code: NHA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.K253922Neodent Scannable Healing AbutmentJJGC Indústria e Comércio de Materiais Dentários S.A.K254145Omni-Directional Multi-Unit Abutment System (Trade Name: Omnibut™)Smart Denture Conversions, LLC

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.

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