CLEAR-LOCK CERAMIC 466-722

GUDID D9094667220

022 U3L CLEAR-LOCK CERAMIC ACTIVE SLB - ROTH HK (5)

Ortho Arch Company Inc

Non-antimicrobial wound irrigation solution, multiple solute

• Primary Device ID: D9094667220
• NIH Device Record Key: b9489154-9564-42ac-bd57-8a85d4f7dcc2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLEAR-LOCK CERAMIC
• Version Model Number: 466-722
• Catalog Number: 466-722
• Company DUNS: 020956330
• Company Name: Ortho Arch Company Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• 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
HIBCC	D9094667220 [Primary]

FDA Product Code

• NJM: Bracket, Ceramic, Orthodontic

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: 2023-07-05
• Device Publish Date: 2023-06-27

On-Brand Devices [ CLEAR-LOCK CERAMIC]

• D9094668450: 022 LRA CLEAR-LOCK CERAMIC ACTIVE SLB - MBT (5)
• D9094668320: 022 UBIL CLEAR-LOCK CERAMIC ACTIVE SLB - MBT HK (5)
• D9094667510: 022 L3R CLEAR-LOCK CERAMIC ACTIVE SLB - ROTH HK (5)
• D9094667220: 022 U3L CLEAR-LOCK CERAMIC ACTIVE SLB - ROTH HK (5)
• D9094667120: 022 U2L CLEAR-LOCK CERAMIC ACTIVE SLB - ROTH (5)