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Bone Grafting Material, Human Source

FDA product code NUN · Class 2 · Dental

163

Registered devices

121

Adverse events

0

Recalls

15

510(k) clearances

Devices with this code

GRAFTON® DBM — MEDTRONIC SOFAMOR DANEK, INC.SurFuse II Putty — Hans Biomed Corp.C-Blast Putty — Hans Biomed Corp.OpteCure+CCC — Exactech, Inc.C-Blast Putty — Hans Biomed Corp.PROGENIX® PUTTY and PROGENIX® PLUS — MEDTRONIC SOFAMOR DANEK, INC.Accell Connexus — KEYSTONE DENTAL, INC.DynaBlast — KEYSTONE DENTAL, INC.RegenaVate™ Formable DBM, 1cm x 4cm x 0.5cm, 2cc — Rti Surgical, Inc.C-Graft Putty — Hans Biomed Corp.GRAFTON®and GRAFTON PLUS®Demineralized Bone Matrix (DBM) — MEDTRONIC SOFAMOR DANEK, INC.REGENEROSS® — ZimVie US Corp LLC Salvin Dental Specialties — SALVIN DENTAL SPECIALTIES, LLC SurFuse II Putty — Hans Biomed Corp.DynaGraft D — KEYSTONE DENTAL, INC.GRAFTON® DBM — MEDTRONIC SOFAMOR DANEK, INC.TruForm — Hans Biomed Corp.Beta-bsm ® — Etex Corporation TruForm+ — Hans Biomed Corp.TruForm+ — Hans Biomed Corp.TruForm — Hans Biomed Corp.TruForm — Hans Biomed Corp.GRAFTON® DBM — MEDTRONIC SOFAMOR DANEK, INC.TruForm — Hans Biomed Corp.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.