FDA UDI In Commercial Distribution 🇺🇸 United States

Ossera™ AFX Instrumentation

DI: 00840097534428 · Model: 5741-3600 · Restor3d, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ossera™ AFX Instrumentation
Primary DI
00840097534428
Version / Model
5741-3600
Company Name
Restor3d, Inc.
Labeler DUNS
080819836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-18
Public Version
1
Public Version Date
2025-12-26
Public Version Status
New
Public Device Record Key
ef20b02d-b6db-48e6-a83c-e0c821e5ae2b

Device Description

Ossera AFX™ Trial, Dome, 36D

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
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
SAI Ankle Fusion Cage

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00840097534428

Premarket Submissions

Submission Number Supplement Number
K242356 000