FDA UDI In Commercial Distribution 🇺🇸 United States

CurvaFix Redirect System Instrument Set

DI: 10850070500712 · Model: CIS-008-LP · CURVAFIX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CurvaFix Redirect System Instrument Set
Primary DI
10850070500712
Version / Model
CIS-008-LP
Catalog Number
CIS-008-LP
Company Name
CURVAFIX, INC.
Labeler DUNS
039779098
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-14
Public Version
1
Public Version Date
2026-04-22
Public Version Status
New
Public Device Record Key
2173efb8-ea8b-462c-80a7-5412d119d0dc

Device Description

A reusable instrument set consisting of the Redirect Handle, housed in a sterilizable storage container, that is used during a surgical procedure for the CurvaFix Low Profilie Implant. Provided non-sterile; ready for cleaning and steam sterilization at healthcare facility before use; reprocessed after each use. See below for kit item descriptions.

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

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 10850070500712

Customer Contacts

Phone
4252768800