FDA UDI Not in Commercial Distribution 🇺🇸 United States

Preference 2

DI: M555159000331 · Model: H · SINTX Technologies, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Preference 2
Primary DI
M555159000331
Version / Model
H
Catalog Number
15-9000-331
Company Name
SINTX Technologies, Inc.
Labeler DUNS
028629553
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-29
Public Version
6
Public Version Date
2026-03-20
Public Version Status
Update
Public Device Record Key
d11472cb-9918-4844-aafe-02f8b285c621
Distribution End Date
2024-11-14

Device Description

5.5mm Caddy Lid

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
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary M555159000331

Customer Contacts

Phone
801-839-3500