FDA 510(k)

CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO

K-Number: K051443 · 2005-07-22

Decision Date2005-07-22

Product CodeLYC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO is the device name listed in this FDA 510(k) record. The listed applicant is Curasan Ag, Frankfurt Facility. It received FDA 510(k) clearance on 2005-07-22 under 510(k) number K051443. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO?

CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO is a medical device that received FDA 510(k) clearance on 2005-07-22. The listed applicant is Curasan Ag, Frankfurt Facility. The 510(k) number is K051443.

When did CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO receive FDA 510(k) clearance?

CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO received FDA 510(k) clearance on 2005-07-22, under 510(k) number K051443.

Who is the listed applicant for CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO?

The FDA 510(k) record lists Curasan Ag, Frankfurt Facility as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO?

The FDA product code for CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO is LYC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: LYC)

K253317Cytrans™ ElashieldGC America, Inc.K253883Bonalive MaxillofacialBonalive , Ltd.K251818BONTREE PLUSHudens Bio Co., Ltd.K244006FG Bone Graft MFull Golden Biotech Co., Ltd.K243745FG Bone Graft BFull Golden Biotech Corporation K241186Synthetic Bone Graft ParticulateShenzhen Dazhou Medical Technology Co., Ltd.

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.