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FDA 510(k)

Multi-Unit DAS System

K-Number: K243732 · 2026-01-29

ApplicantTalladium España, SL
Decision Date2026-01-29
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Multi-Unit DAS System is a medical device manufactured by Talladium España, SL. It received FDA 510(k) clearance on 2026-01-29 under approval number K243732. 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 2026-01-29. It is manufactured by Talladium España, SL. The 510(k) number is K243732.

When was Multi-Unit DAS System approved by the FDA?

Multi-Unit DAS System received FDA 510(k) clearance on 2026-01-29, under approval number K243732.

What company makes Multi-Unit DAS System?

Multi-Unit DAS System is manufactured by Talladium España, SL.

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

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

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Related PubMed Literature

PMID: 42168293 Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling. Scientific reports (2026)

Other Devices by Talladium España, SL

K212108Dynamic TiBase K231559Multi-Unit DAS System K232151Dynamic TiBase K241170Dynamic TiBase; TRI Screws K243425Guided DAS Surgical Kit K243530Dynamic TiBase

View all 7 devices →

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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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