FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoMTA

DI: 08800027200078 · Model: OM50 · BioMTA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
OrthoMTA
Primary DI
08800027200078
Version / Model
OM50
Company Name
BioMTA
Labeler DUNS
694860083
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-22
Public Version
4
Public Version Date
2024-04-10
Public Version Status
Update
Public Device Record Key
78b5718e-7ecf-4b3a-8563-0df40ff97ed7

Device Description

OrthoMTA is ideal for orthograde root canal grafting material especially for file separation, crack tooth syndrome, severely infected canal, and re-endo of acute periapical abscess. Furthermore, OrthoMTA has a wide variety of clinical indications such as for apexification, repair of root perforations, and internal root resporption.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KIF Resin, Root Canal Filling

GMDN Terms

Code Name
36095 Endodontic filling/sealing material

Identifiers

Type ID
Primary 08800027200078

Premarket Submissions

Submission Number Supplement Number
K102575 000