Cap Remover 100-701

GUDID 00190746067488

INSTRUMENT REPLACEMENT BLADES FOR CAP REMOVER 10/PKG

AMERICAN ORTHODONTICS CORPORATION

Orthodontic pliers

• Primary Device ID: 00190746067488
• NIH Device Record Key: 4673511d-8d7b-4548-ad44-dac8713af806
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cap Remover
• Version Model Number: 100-701
• Catalog Number: 100-701
• Company DUNS: 044668515
• Company Name: AMERICAN ORTHODONTICS CORPORATION
• 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: false
• Lot Batch: true
• Serial Number: false
• 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

Customer Support Contacts

• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com
• Phone: +1(800)558-7687
• Email: info@americanortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190746067488 [Primary]

FDA Product Code

• DZN: INSTRUMENTS, DENTAL HAND

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: 2026-02-05
• Device Publish Date: 2026-01-28

Devices Manufactured by AMERICAN ORTHODONTICS CORPORATION

• 00190746067280 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS MBT 022 U/L 7X7 IFIT W/HK 3,4,5 STICKY
• 00190746070761 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS ROTH 022 U/L 7X7 IFIT W/HK 3,4,5 STICKY
• 00190746070785 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS ROTH 022 U/L 6X6 IFIT W/HK 3,4,5 STICKY
• 00190746070808 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS ROTH 018 U/L 7X7 IFIT W/HK 3,4,5 STICKY
• 00190746070822 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS ROTH 022 U/L 5X5 W/HK 3 STICKY 197 PAD
• 00190746070853 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS ROTH 022 U/L 5X5 W/HK 3,4,5 STICKY 197 PAD
• 00190746070860 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS MBT 022 U/L 5X5 W/HK 3 UL3 T=0 STICKY 197 PAD
• 00190746070891 - Mini Master Series Bracket: 2026-02-27 1 PAT SETUP MINI MS MBT 022 U/L 5X5 W/HK 3,4,5 UL3 T=0 STICKY 197 PAD