FDA UDI In Commercial Distribution 🇺🇸 United States

MEDENTiKA

DI: EMKAL26102 · Model: L 2610-2 · MEDENTiKA GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MEDENTiKA
Primary DI
EMKAL26102
Version / Model
L 2610-2
Company Name
MEDENTiKA GmbH
Labeler DUNS
537555497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-30
Public Version
5
Public Version Date
2022-11-14
Public Version Status
Update
Public Device Record Key
5b15f30b-f095-4276-9a8e-1c93b3958606

Device Description

MedentiLOC abutment

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NHA ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary EMKAL26102

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142167 000

Device Sizes

Type Value Unit Text
Device Size Text, specify angled ; Compatible with Implant System : Straumann® / Bone Level® ; RC 4,1/4,8
Angle 15 degree