FDA UDI In Commercial Distribution 🇺🇸 United States

LEONE SPA

DI: 08033707096320 · Model: 002-1708P04 · LEONE SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LEONE SPA
Primary DI
08033707096320
Version / Model
002-1708P04
Catalog Number
002-1708P04
Company Name
LEONE SPA
Labeler DUNS
432167294
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-07
Public Version
3
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
2c10e92b-8a5b-4d05-8688-fb102df4754f

Device Description

MINI IMPL SELF-DRILL W/SLOT HIGHD1,75 L8

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OAT Implant, Endosseous, Orthodontic

GMDN Terms

Code Name
46536 Orthodontic anchoring screw

Identifiers

Type ID
Primary 08033707096320

Premarket Submissions

Submission Number Supplement Number
K071490 000