Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FG Bone Graft B

K-Number: K243745 · 2025-08-29

ApplicantFull Golden Biotech Corporation
Decision Date2025-08-29
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FG Bone Graft B is a medical device manufactured by Full Golden Biotech Corporation. It received FDA 510(k) clearance on 2025-08-29 under approval number K243745. 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 FG Bone Graft B?

FG Bone Graft B is a medical device that received FDA 510(k) clearance on 2025-08-29. It is manufactured by Full Golden Biotech Corporation. The 510(k) number is K243745.

When was FG Bone Graft B approved by the FDA?

FG Bone Graft B received FDA 510(k) clearance on 2025-08-29, under approval number K243745.

What company makes FG Bone Graft B?

FG Bone Graft B is manufactured by Full Golden Biotech Corporation.

What is the FDA product code for FG Bone Graft B?

The FDA product code for FG Bone Graft B is LYC.

Related Devices (Code: LYC)

K153676OSTEON IIIGenoss Co., Ltd. K153230ShefaBone SCPC Resorbable Bone GraftThe Implantech Inc./Shefabone K201546OsOpia Synthetic Bone Void FillerRevisios BV K201051Straumann BoneCeramicInstitut Straumann AG K192597Cytrans GranulesGC America, Inc. K213260CMFlexTMDimension Inx Corp.

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.

↑