Collagen P.I.N.

GUDID 00850021673055

Microneedling Device Handpiece (Single)

Induction Therapies, LLC

Cosmetic micro-needling electronic handpiece, professional

• Primary Device ID: 00850021673055
• NIH Device Record Key: 2468e6c2-03ea-4c33-8c16-d7701208d64e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Collagen P.I.N.
• Version Model Number: 1
• Company DUNS: 098256562
• Company Name: Induction Therapies, LLC
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850021673055 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222199

FDA Product Code

• QAI: Powered Microneedle Device

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: 2023-03-20
• Device Publish Date: 2023-03-11

On-Brand Devices [Collagen P.I.N.]

• 00196852959570: Microneedling Device
• 00196852440313: 1
• 00850021673024: 36 Pin Needle Cartridge
• 00850021673017: Microneedling Device
• 00850021673031: 24 Pack - 36 Pin Microneedling Cartridge
• 00850021673048: 100 Pack - 36 Pin Microneedling Cartridge
• 00850021673062: Microneedling Device Kit (Partial)
• 00850021673055: Microneedling Device Handpiece (Single)
• 00850021673079: Microneedling Device Kit (Ocean)