FDA UDI In Commercial Distribution 🇺🇸 United States

Osstell Beacon Instrument

DI: 09010522002650 · Model: Osstell Beacon Instrument · Osstell AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Osstell Beacon Instrument
Primary DI
09010522002650
Version / Model
Osstell Beacon Instrument
Catalog Number
103000
Company Name
Osstell AB
Labeler DUNS
633171269
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-26
Public Version
1
Public Version Date
2025-10-06
Public Version Status
New
Public Device Record Key
59506596-0908-4611-923a-75f029f3c751

Device Description

ISQ Measurement Instrument

Device Characteristics

Single Use
No
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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKX Handpiece, Direct Drive, Ac-Powered

GMDN Terms

Code Name
63467 Dental implant stability resonance frequency analysis unit

Identifiers

Type ID
Primary 09010522002650
Package 09010522002643

Premarket Submissions

Submission Number Supplement Number
K181888 000