FDA UDI In Commercial Distribution 🇺🇸 United States

Ax®

DI: M711LS3350 · Model: LS-335 · INNO Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ax®
Primary DI
M711LS3350
Version / Model
LS-335
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-31
Public Version
2
Public Version Date
2025-12-17
Public Version Status
Update
Public Device Record Key
96de5142-62dc-4edf-abdb-f52d73bcc254

Device Description

Anterior Cup Curette, Straight, Size 2, Al, Silicone, SST

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
HTF Curette

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary M711LS3350

Customer Contacts

Phone
801-261-2236