Collagen P.I.N.

GUDID 00196852959570

Microneedling Device

Induction Therapies, LLC

Cosmetic micro-needling electronic handpiece, professional

• Primary Device ID: 00196852959570
• NIH Device Record Key: 8b0f901e-cf94-4143-bb7a-f35a43eac1f3
• 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: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• 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	00196852959570 [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: 2022-11-24
• Device Publish Date: 2022-11-16

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)