Primary Device ID | D768RS3813K0 |
NIH Device Record Key | fca2f691-637b-44b9-a69b-421d0a461eb9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Restore Implant System |
Version Model Number | RS3813K |
Catalog Number | RS3813K |
Company DUNS | 787471015 |
Company Name | KEYSTONE DENTAL, 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 | 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(781)328-3515 |
cyoung@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D768RS3813K0 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | true |
Device Is Sterile | true |
[D768RS3813K0]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-01-29 |
D768TS5013K0 | Implant |
D768TS5011K0 | Implant |
D768TS5010K0 | Implant |
D768TS4015UK0 | Implant |
D768TS4015K0 | Implant |
D768TS4013UK0 | Implant |
D768TS4013K0 | Implant |
D768TS4011UK0 | Implant |
D768TS4011K0 | Implant |
D768TS4010UK0 | Implant |
D768TS4010K0 | Implant |
D768TS4008K0 | Implant |
D768TS3815UK0 | Implant |
D768TS3815K0 | Implant |
D768TS3813UK0 | Implant |
D768TS3813K0 | Implant |
D768TS3811UK0 | Implant |
D768TS3811K0 | Implant |
D768TS3810UK0 | Implant |
D768TS3810K0 | Implant |
D768TS3808K0 | Implant |
D768TS3315K0 | Implant |
D768TS3313K0 | Implant |
D768TS3311UK0 | Implant |
D768TS3311K0 | Implant |
D768TS3310K0 | Implant |
D768RS6015K0 | Implant |
D768RS6013K0 | Implant |
D768RS6011K0 | Implant |
D768RS6010K0 | Implant |
D768RS6008K0 | Implant |
D768RS5015K0 | Implant |
D768RS5013UK0 | Implant |
D768RS5013K0 | Implant |
D768RS5011UK0 | Implant |
D768RS5011K0 | Implant |
D768RS5010UK0 | Implant |
D768RS5010K0 | Implant |
D768RS5008K0 | Implant |
D768RS4015UK0 | Implant |
D768RS4015K0 | Implant |
D768RS4013UK0 | Implant |
D768RS4013K0 | Implant |
D768RS4011UK0 | Implant |
D768RS4011K0 | Implant |
D768RS4010UK0 | Implant |
D768RS4010K0 | Implant |
D768RS4008K0 | Implant |
D768RS4006K0 | Implant |
D768RS3815UK0 | Implant |