FDA UDI Not in Commercial Distribution 🇺🇸 United States

Gibralt®

DI: M711050021335700 · Model: 05-002-13-3570 · INNO Holdings, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Gibralt®
Primary DI
M711050021335700
Version / Model
05-002-13-3570
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-29
Public Version
4
Public Version Date
2025-12-19
Public Version Status
Update
Public Device Record Key
70aabf12-3b31-40dd-8c77-0ca000721e22
Distribution End Date
2025-12-18

Device Description

Posterior Cervical, Rod, Prebent, CoCr, 3.5mm x 70mm, Co 28Cr 6Mo

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
NKG Posterior Cervical Screw System
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
65116 Bone-screw internal spinal fixation system rod

Identifiers

Type ID
Primary M711050021335700

Customer Contacts

Phone
801-261-2236

Device Sizes

Type Value Unit Text
Length 70 Millimeter
Outer Diameter 3.5 Millimeter