FDA UDI In Commercial Distribution 🇺🇸 United States

BoneFoam

DI: 00810075280753 · Model: 925.KBEX-BX4 · BONE FOAM, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

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Basic Information

Brand Name
BoneFoam
Primary DI
00810075280753
Version / Model
925.KBEX-BX4
Catalog Number
925.KBEX-BX4
Company Name
BONE FOAM, INC.
Labeler DUNS
079636174
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2022-05-22
Public Version
2
Public Version Date
2023-04-11
Public Version Status
Update
Public Device Record Key
02065a75-ba54-4eba-95f0-389705f4be8d

Device Description

Knee Buddy Extender - Box of 4

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
No

Product Codes

Code Name
IQI ORTHOSIS, LIMB BRACE

GMDN Terms

Code Name
41542 Leg/knee cushion

Identifiers

Type ID
Unit of Use 00810075281187
Primary 00810075280753