PEACH 2 go

GUDID 07350120791900

PEACH™ 2 go is an over-the-counter device intended for the removal of unwanted body hair and/or facial hair.

Foreo AB

Home-use intense pulsed light hair removal unit

• Primary Device ID: 07350120791900
• NIH Device Record Key: a6e44d45-14ef-46f3-9364-362ef51a547a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PEACH 2 go
• Version Model Number: Peach
• Company DUNS: 352394143
• Company Name: Foreo AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350120791900 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231977

FDA Product Code

• OHT: Light Based Over-The-Counter Hair Removal

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-15
• Device Publish Date: 2024-08-07

On-Brand Devices [PEACH 2 go]

• 07350120791894: PEACH 2 duo is an over-the-counter device intended for the removal of unwanted body hair and/or
• 07350120791917: PEACH™ 2 go is an over-the-counter device intended for the removal of unwanted body hair and/o
• 07350120791900: PEACH™ 2 go is an over-the-counter device intended for the removal of unwanted body hair and/o