FDA UDI In Commercial Distribution 🇺🇸 United States

Osseolive Dental

DI: ECURL05M0250 · Model: 250-1000µm · curasan AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Osseolive Dental
Primary DI
ECURL05M0250
Version / Model
250-1000µm
Catalog Number
5 x 0.5 cc
Company Name
curasan AG
Labeler DUNS
324331826
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2017-10-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
45df2a50-9eb5-461f-b0f2-cac0ace241f2

Device Description

Device Name: Curasan OSSEOLIVE® DENTAL lndications for Use: OSSEOLIVE® DENTAL is indicated for applications in oral and maxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled (artificial or degenerative) bone defects, e.g.: - Defects after the extirpation of bone cysts - Augmentation of an atrophied alveolar ridge - Sinus lift or sinus floor elevation (subantral augmentation) - Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge - Filling of extraction defects to create an implant bed - Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects - Defects after operative removal of retained teeth or corrective osteotomies

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
47971 Dental bone matrix implant, synthetic

Identifiers

Type ID
Primary ECURL05M0250
Unit of Use ECURL05M02505

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111105 000