FDA UDI In Commercial Distribution 🇺🇸 United States

Kinos Aeros Instrumentation

DI: 00840097513164 · Model: 5871-0016 · Restor3d, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Kinos Aeros Instrumentation
Primary DI
00840097513164
Version / Model
5871-0016
Company Name
Restor3d, Inc.
Labeler DUNS
080819836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-09
Public Version
1
Public Version Date
2026-04-17
Public Version Status
New
Public Device Record Key
9c1db9d9-5708-40c9-b446-0e97f17ca733

Device Description

16mm Flexible Reamer, Sterile

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HSN Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary 00840097513164

Premarket Submissions

Submission Number Supplement Number
K242868 000