Duns Number:675938472
Device Description: truSculpt flex comprises a system console with touchscreen LCD and sixteen electrode handp truSculpt flex comprises a system console with touchscreen LCD and sixteen electrode handpieces, which deliver electrical impulses to the skin in direct proximity to the muscles to be stimulated. The electrical impulses are delivered in the subdermal muscular tissue area, triggering comforting and soothing muscle stimulation to achieve the intended use of strengthening, firming, and toning the muscles of the abdomen, thighs, and buttocks.
Catalog Number
-
Brand Name
Johari Digital Healthcare Ltd.
Version/Model Number
truSculpt Flex
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
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For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K131291
Product Code
NGX
Product Code Name
Stimulator, Muscle, Powered, For Muscle Conditioning
Public Device Record Key
1e8dcd81-37fd-4f56-aef9-5e5b050477cf
Public Version Date
February 19, 2021
Public Version Number
4
DI Record Publish Date
June 21, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 41 |
| 3 | A medical device with high risk that requires premarket approval | 1 |