510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K952922Substantially Equivalent

Biogran Bioactive Glass Synthetic Bone Graft Material

DSM Biomedical, Inc., Princeton NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952922 is the FDA 510(k) clearance record for BIOGRAN BIOACTIVE GLASS SYNTHETIC BONE GRAFT MATERIAL, a class II device, cleared for Orthovita Co. on under FDA product code LYC (Bone Grafting Material, Synthetic). FDA's definition for product code LYC reads: "A synthetic bone grafting material is synthetically-derived device, such as hydroxylapatite, intended to fill, augment, or reconstruct periodontal and or bony defects of the upper or lower jaw". FDA records list 54 510(k) clearances for DSM Biomedical, Inc., from to . As of , FDA records show no recalls naming K952922.

Clearance record

Decision date
Received
(176 days to decision)
Product code
LYC Bone Grafting Material, Synthetic
Regulation
21 CFR 872.3930
Device class
Class II
Review panel
Dental
Applicant
Orthovita Co. 212 Carnigie Center Dr., Princeton NJ
510(k) summary
Summary
Third party review
No

Clearances, product code LYC

Trailing 12 months
3 clearances under product code LYC in the twelve months to November 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LYC, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20261
August 20260
September 20260
October 20260
November 20260