Primary Device ID | 00647529004296 |
NIH Device Record Key | 1736febe-7c1d-47a5-abf5-b03cab6874ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EdgePro |
Version Model Number | Tip Assembly - One-17 mm |
Catalog Number | 6200155 |
Company DUNS | 152165700 |
Company Name | Biolase, Inc. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
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 | 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 |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com | |
Phone | 1-800-321-6717 |
Waterlaseservice@biolase.com |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Length | 17 Millimeter |
Outer Diameter | 200 Micrometer |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00647529003565 [Package] Package: Box [10 Units] In Commercial Distribution |
GS1 | 00647529004289 [Package] Package: Box [30 Units] In Commercial Distribution |
GS1 | 00647529004296 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
[00647529004296]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-27 |
Device Publish Date | 2023-06-19 |
00647529004296 | A reusable fiberoptic tip accessory intended for use with EdgePro Laser System (Juno). |
00647529004241 | A reusable handpiece intended for use with the EdgePro Laser System (Juno) in a variety of denta |
00647529004135 | An all-tissue dental laser system intended for a variety of oral soft-tissue and hard-tissue pro |
00647529004326 | A reusable fiberoptic tip accessory intended for use with EdgePro Laser System (Juno). |
00647529003572 | A reusable fiberoptic tip accessory intended for use with EdgePro Laser System (Juno). |
00647529004180 | A reusable fiberoptic tip accessory intended for use with EdgePro Laser System (Juno). |
00647529003589 | A reusable fiberoptic tip accessory intended for use with EdgePro Laser System (Juno). |
00647529004319 | A reusable fiberoptic tip accessory intended for use with EdgePro Laser System (Juno). |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EDGEPRO 98759467 not registered Live/Pending |
National Nail Corp. 2024-09-19 |
EDGEPRO 97856460 not registered Live/Pending |
Currex GmbH 2023-03-24 |
EDGEPRO 97662659 not registered Live/Pending |
Progress Engineering, LLC 2022-11-04 |
EDGEPRO 97566708 not registered Live/Pending |
Litco Corner Protection, LLC 2022-08-26 |
EDGEPRO 90200630 not registered Live/Pending |
Edge Endo, LLC 2020-09-22 |
EDGEPRO 87874838 5575949 Live/Registered |
Gateway Professional Network, LLC 2018-04-12 |
EDGEPRO 86910532 not registered Dead/Abandoned |
Guardian Protection Services, Inc. 2016-02-17 |
EDGEPRO 85806152 4372478 Live/Registered |
currex GmbH 2012-12-19 |
EDGEPRO 85389162 4201058 Dead/Cancelled |
THE VOLLRATH COMPANY, L.L.C. 2011-08-04 |
EDGEPRO 78123595 2783243 Dead/Cancelled |
3M COMPANY 2002-04-23 |
EDGEPRO 74663508 not registered Dead/Abandoned |
Visual Edge Technology 1995-04-20 |
EDGEPRO 74272094 1822774 Live/Registered |
DIMEX LLC 1992-05-04 |