Primary Device ID | 10841307113041 |
NIH Device Record Key | 9da84256-37e8-4ccc-aa79-413d79367a82 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RePlant® Cover Screw |
Version Model Number | 6060-01 |
Catalog Number | 6060-01 |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
Device Count | 1 |
DM Exempt | false |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841307113041 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-09-14 |
10841307113041 | 6060-01 |
10841307113034 | 6050-01 |
10841307113027 | 6043-01 |
10841307113010 | 6035-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() REPLANT 97914673 not registered Live/Pending |
Von Holzhausen 2023-05-01 |
![]() REPLANT 97914671 not registered Live/Pending |
Von Holzhausen 2023-05-01 |
![]() REPLANT 97036376 not registered Live/Pending |
Strange Attractor, LLC 2021-09-20 |
![]() REPLANT 88518101 not registered Live/Pending |
Michelle MacRae 2019-07-17 |
![]() REPLANT 77097406 not registered Dead/Abandoned |
Implant Direct LLC 2007-02-01 |
![]() REPLANT 76628186 3344697 Live/Registered |
IMPLANT DIRECT SYBRON INTERNATIONAL LLC 2005-01-19 |