FDA UDI In Commercial Distribution 🇺🇸 United States

Patient-Fitted TMJ Reconstructive Prosthesis System

DI: 07613327626735 · Model: 60-0520 · TMJ Solutions, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Patient-Fitted TMJ Reconstructive Prosthesis System
Primary DI
07613327626735
Version / Model
60-0520
Company Name
TMJ Solutions, Inc.
Labeler DUNS
035877922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-11
Public Version
1
Public Version Date
2023-09-19
Public Version Status
New
Public Device Record Key
5b3d4b6c-f4fc-4407-b9fa-92b8e960fe63

Device Description

Sterilization Case Instrument Base

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Primary 07613327626735
Previous B0046005200

Customer Contacts

Phone
805-650-3391