510(k) K253883

Device
Bonalive Maxillofacial
Applicant
Bonalive , Ltd.
510(k) number
K253883
Product code
LYC
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-14
Date received
2025-12-04
Regulation
872.3930
Classification name
Bone Grafting Material, Synthetic
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Jenna Saarimäki
Address
Biolinja 2 Turku FI 20750 20750

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LYC#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K251818BONTREE PLUSHudens Bio Co., Ltd.2026-03-06
K244006FG Bone Graft MFull Golden Biotech Co., Ltd.2025-09-17
K243745FG Bone Graft BFull Golden Biotech Corporation2025-08-29
K241186Synthetic Bone Graft ParticulateShenzhen Dazhou Medical Technology Co., Ltd.2025-02-21
K213260CMFlexTMDimension Inx Corp.2022-12-30
K202675InRoad® Dental Synthetic Bone GraftOsteogene Tech Corp2022-03-04
K201546OsOpia Synthetic Bone Void FillerRevisios BV2020-10-02
K201051Straumann BoneCeramicInstitut Straumann AG2020-09-24
K192597Cytrans GranulesGC America, Inc.2020-08-17
K153676OSTEON IIIGenoss Co., Ltd.2016-09-14
K153230ShefaBone SCPC Resorbable Bone GraftThe Implantech Inc./Shefabone2016-07-14
K140374MASTERGRAFT PUTTYMedtronic Sofamor Danek USA, Inc.2014-06-10
K121177BOND APATITEAugma Biomaterials, Ltd.2013-12-05
K131385EASY-GRAFTDegradable Solutions AG2013-09-27
K111105CURASAN OSSEOLIVE DENTALCurasan AG2012-12-20