SPONGE PELLET

GUDID 00840479203447

RELIANCE ORTHODONTIC PRODUCTS INC

Dental material application tool, single-use

• Primary Device ID: 00840479203447
• NIH Device Record Key: 4acd3d1d-69ab-47e4-aa75-429ac3842014
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPONGE PELLET
• Version Model Number: SP
• Company DUNS: 113170088
• Company Name: RELIANCE ORTHODONTIC PRODUCTS 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840479203447 [Primary]

FDA Product Code

• ECP: Instrument, Ligature Tucking, 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: 2026-03-20
• Device Publish Date: 2026-03-12

On-Brand Devices [SPONGE PELLET]

• 00840479200651: 1SP
• 00840479203447: SP