FDA UDI In Commercial Distribution 🇺🇸 United States

restor3d Cervical Cage

DI: 00840097500546 · Model: 1110-16130600 · Restor3d, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
restor3d Cervical Cage
Primary DI
00840097500546
Version / Model
1110-16130600
Company Name
Restor3d, Inc.
Labeler DUNS
080819836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-17
Public Version
3
Public Version Date
2025-07-14
Public Version Status
Update
Public Device Record Key
450413eb-f62b-4a90-ae25-4bd7b766cf24

Device Description

Titanium (Ti-6Al-4V) Cervical Cage, 16Wx13Dx6Hx0

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
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00840097500546

Premarket Submissions

Submission Number Supplement Number
K191812 000