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

FDA 510(k)

DSM Biomedical Dental Bone Graft

K-Number: K170245 · 2017-05-16

ApplicantKensey Nash Corporation Dba Dsm Biomedical
Decision Date2017-05-16
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DSM Biomedical Dental Bone Graft is the device name listed in this FDA 510(k) record. The listed applicant is Kensey Nash Corporation Dba Dsm Biomedical. It received FDA 510(k) clearance on 2017-05-16 under 510(k) number K170245. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSM Biomedical Dental Bone Graft?

DSM Biomedical Dental Bone Graft is a medical device that received FDA 510(k) clearance on 2017-05-16. The listed applicant is Kensey Nash Corporation Dba Dsm Biomedical. The 510(k) number is K170245.

When did DSM Biomedical Dental Bone Graft receive FDA 510(k) clearance?

DSM Biomedical Dental Bone Graft received FDA 510(k) clearance on 2017-05-16, under 510(k) number K170245.

Who is the listed applicant for DSM Biomedical Dental Bone Graft?

The FDA 510(k) record lists Kensey Nash Corporation Dba Dsm Biomedical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DSM Biomedical Dental Bone Graft?

The FDA product code for DSM Biomedical Dental Bone Graft is NPM.

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.

NCT06533397The Application of a Biphasic Calcium Sulfate Graft Material in Sinus Floor ElevationRECRUITINGNCT07091448Biotivity A-C Membrane Socket Preservation StudyNOT_YET_RECRUITINGNCT07381608Clinical and Patient-reported Outcomes of Guided Versus Freehand Harvesting Of Positioning of Autogenous Bone ShellsCOMPLETEDNCT07512011Outcomes of Different Bone Graft Combinations for Maxillary Sinus Augmentation ProcedureNOT_YET_RECRUITINGNCT07569146Assessment of Deproteinized Bovine Bone for Immediate Implants Placement in Maxillary Esthetic Zone.COMPLETEDNCT07580495Effect of Collagen Membrane on Ridge PreservationRECRUITING

Other records listing Kensey Nash Corporation Dba Dsm Biomedical 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.

K173572DSM Biomedical Calcium Phosphate Cement with MicrospheresK173362DSM Biomedical Calcium Phosphate CementK160474DSM Biomedical Porcine Pericardium Dental Membrane

Related Devices (Code: NPM)

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.

K253723BOSSMedpark Co., Ltd.K251786Geistlich Bio-Oss®; Geistlich Bio-Oss Pen®Geistlich Pharma AGK251613SwissGraft XGeistlich Pharma AGK242510Geistlich Bio-Flow®Geistlich Pharma AGK240133Xenograft Bovine Bone ParticulateCollagen Solutions, LLCK230305THE Graft CollagenPurgo Biologics, Inc.

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.

↑