NexxZr™ Plus / W-98-12-NP-D200-SD

GUDID 00814356021554

https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=678281#deviceRecordKey=677511#

SAGEMAX BIOCERAMICS, INC

Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic Dental appliance fabrication material, ceramic
Primary Device ID00814356021554
NIH Device Record Key7223db20-17d1-45cd-aa77-68b0c33500c3
Commercial Distribution StatusIn Commercial Distribution
Brand NameNexxZr™ Plus / W-98-12-NP-D200-SD
Version Model NumberW-22145
Company DUNS002265727
Company NameSAGEMAX BIOCERAMICS, INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100814356021554 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EIHPowder, Porcelain

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-24
Device Publish Date2018-03-26

Devices Manufactured by SAGEMAX BIOCERAMICS, INC

00842271158666 - NexxZr Plus Multi 2.0 B3 W98-20mm2024-03-28
00842271158673 - NexxZr Plus Multi 2.0 B4 W98-20mm2024-03-28
00842271158680 - NexxZr Plus Multi 2.0 C1 W98-20mm2024-03-28
00842271158697 - NexxZr Plus Multi 2.0 C2 W98-20mm2024-03-28
00842271158703 - NexxZr Plus Multi 2.0 C3 W98-20mm2024-03-28
00842271158710 - NexxZr Plus Multi 2.0 C4 W98-20mm2024-03-28
00842271158727 - NexxZr Plus Multi 2.0 D2 W98-20mm2024-03-28
00842271158734 - NexxZr Plus Multi 2.0 D3 W98-20mm2024-03-28

Trademark Results [NexxZr]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NEXXZR
NEXXZR
85234108 4136586 Live/Registered
Sagemax Bioceramics, Inc.
2011-02-04

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.