FDA UDI In Commercial Distribution 🇺🇸 United States

Oryx™

DI: M711AP2340 · Model: AP234 · INNO Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Oryx™
Primary DI
M711AP2340
Version / Model
AP234
Catalog Number
AP234
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-31
Public Version
5
Public Version Date
2025-12-23
Public Version Status
Update
Public Device Record Key
d8fc498c-9f80-4df6-8463-a8111b07b4b4

Device Description

Ti 6Al 4V (ELI)

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary M711AP2340

Customer Contacts

Phone
801-261-2236

Device Sizes

Type Value Unit Text
Length 34 Millimeter