FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoXcell BA

DI: 05060548020231 · Model: OSBA-003 · BIOSTONE CO. LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
OsteoXcell BA
Primary DI
05060548020231
Version / Model
OSBA-003
Catalog Number
OSBA-003
Company Name
BIOSTONE CO. LIMITED
Labeler DUNS
222236587
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-18
Public Version
2
Public Version Date
2025-12-01
Public Version Status
Update
Public Device Record Key
97dc7b10-b476-4f7c-8803-918e84eaa537

Device Description

Silica induced bi-phase calcium phosphate ceramic morsels, 80% HA and 20% beta-TCP size 1 to 2mm volume 3 cc suspended in a biocompatible hydrogel solution packed in a 14ml open bore syringe. They are packed in a vacuum sealed foil inner pouch within a Tyvek outer pouch and packed in a carton box

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 05060548020231