AccessGUDID - DEVICE: Ultra Band Lok (D798NFLLUBLPP0)

GUDID

Device Identifier (DI) Information

Brand Name: Ultra Band Lok
Version or Model: NFLLUBLPP
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: NFLLUBLPP
Company Name: RELIANCE ORTHODONTIC PRODUCTS INC

Primary DI Number: D798NFLLUBLPP0
Issuing Agency: HIBCC
Commercial Distribution End Date: April 25, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 113170088 *Terms of Use

Device Description: Ultra Band-Lok® is intended for use as an orthodontic band cement and for occlusal buildups. This product is Natural shade. This product is Non-Fluoride. This product is a Luer Lok Syringe with Tips.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35870	Dental composite resin	A non-sterile substance intended for professional use as a dental luting agent, liner, base, pulp-capping material, pit/fissure sealant, and/or direct dental restorative material, whereby the majority of the setting reaction is based on the self-, light-, or dual-cured polymerization of a dimethacrylate resin [e.g., polymethylmethacrylate (PMMA), polyurethane, or bisphenol-A-diglycidylether methacrylate (Bis-GMA)]; it includes some additional fillers/components (e.g., glass-based, quartz, or ceramic). It may be preloaded into a syringe, and dedicated disposable devices associated with application may be included. After application, this device cannot be reused.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EBF	Material, Tooth Shade, Resin

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b6fa0dd5-a725-4251-8dcd-2d983b42f344
Public Version Date: April 26, 2019
Public Version Number: 5
DI Record Publish Date: March 24, 2017