FDA UDI In Commercial Distribution 🇺🇸 United States

FUSIO™ SI Allograft System

DI: 00810152100332 · Model: BI0021 · PROMETHEAN RESTORATIVE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FUSIO™ SI Allograft System
Primary DI
00810152100332
Version / Model
BI0021
Catalog Number
BI0021
Company Name
PROMETHEAN RESTORATIVE LLC
Labeler DUNS
124592779
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-13
Public Version
1
Public Version Date
2026-02-23
Public Version Status
New
Public Device Record Key
a91d7dc7-378d-42bc-93aa-28d0241682e3

Device Description

GUIDE TUBE TAP CAP

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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00810152100332

Customer Contacts

Phone
720-512-5947