FDA UDI In Commercial Distribution 🇺🇸 United States

IngeniOS HA

DI: 04260476431319 · Model: 1-2mm · curasan AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IngeniOS HA
Primary DI
04260476431319
Version / Model
1-2mm
Catalog Number
1x1cc
Company Name
curasan AG
Labeler DUNS
324331826
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-30
Public Version
1
Public Version Date
2019-11-07
Public Version Status
New
Public Device Record Key
2818e50b-c5da-4513-8ac0-91176dc50858

Device Description

Device Name: IngeniOS HA Indications for Use: Oral-maxillofacial surgery, dentistry, implantology, periodontology • Defects after removal of bone cysts • Augmentation of the atrophied alveolar ridge • Sinus floor elevation (subantral augmentation) • Filling of alveolar defects following tooth extraction for alveolar ridge preservation • Filling of extraction defects to create an implant bed • Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects • Support function for a membrane in guided tissue regeneration (GTR) • Defects after surgical removal of retained teeth or corrective osteotomies • Other multi-walled bone defects of the alveolar ridge

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LYC Bone Grafting Material, Synthetic

GMDN Terms

Code Name
16966 Synthetic bone graft

Identifiers

Type ID
Primary 04260476431319

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102872 000