FDA UDI In Commercial Distribution 🇺🇸 United States

OraStretch® Press Device – Standard

DI: 00850056079006 · Model: CR1000 · Cranio Mandibular Rehab, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
OraStretch® Press Device – Standard
Primary DI
00850056079006
Version / Model
CR1000
Company Name
Cranio Mandibular Rehab, Inc.
Labeler DUNS
048276773
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-05
Public Version
1
Public Version Date
2023-10-13
Public Version Status
New
Public Device Record Key
61ddb402-96f1-4028-bf77-0b35160fd484

Device Description

The OraStretch press system is indicated for individuals with, or at risk of trismus (limited oral opening) or jaw dysfunction. The appliance may also be used for physical therapy or rehabilitation of the mouth, jaw, or other orofacial tissues. The device is for single-patient use only.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
No

Product Codes

Code Name
ION Exerciser, Non-Measuring

GMDN Terms

Code Name
17802 Mastication muscle exerciser

Identifiers

Type ID
Primary 00850056079006

Customer Contacts

Device Sizes

Type Value Unit Text
Width 60 Millimeter