FDA UDI In Commercial Distribution 🇺🇸 United States

Bone Level Fixture

DI: 00810112920192 · Model: PBF 5008S · Inosys, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bone Level Fixture
Primary DI
00810112920192
Version / Model
PBF 5008S
Company Name
Inosys, Inc.
Labeler DUNS
101803383
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-08
Public Version
1
Public Version Date
2022-06-16
Public Version Status
New
Public Device Record Key
d123b6a4-f3f0-4c7d-bed9-2b4b39c342f6

Device Description

Biotem NON-MICRO THREAD TYPE AR FIXTURE(SLA) Ø5.1 X 8.5mm

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 00810112920192

Premarket Submissions

Submission Number Supplement Number
K190641 000