EM SA IMPLANT (DENTURE)

GUDID 00810019242465

HIOSSEN, INC.

Screw endosteal dental implant, two-piece
Primary Device ID00810019242465
NIH Device Record Key9abf7314-256d-4384-8a9b-040cadadf635
Commercial Distribution StatusIn Commercial Distribution
Brand NameEM SA IMPLANT (DENTURE)
Version Model NumberEMD2015S20
Company DUNS796083090
Company NameHIOSSEN, 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 Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810019242465 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-27
Device Publish Date2019-12-19

On-Brand Devices [EM SA IMPLANT (DENTURE)]

00810019242670EMD3015S40
00810019242663EMD3015S20
00810019242656EMD3013S40
00810019242649EMD3013S20
00810019242632EMD3011S40
00810019242625EMD3011S20
00810019242618EMD3010S40
00810019242601EMD3010S20
00810019242595EMD3008S40
00810019242588EMD3008S20
00810019242571EMD2515S40
00810019242564EMD2515S20
00810019242557EMD2513S40
00810019242540EMD2513S20
00810019242533EMD2511S40
00810019242526EMD2511S20
00810019242519EMD2510S40
00810019242502EMD2510S20
00810019242496EMD2508S40
00810019242489EMD2508S20
00810019242472EMD2015S40
00810019242465EMD2015S20
00810019242458EMD2013S40
00810019242441EMD2013S20
00810019242434EMD2011S40
00810019242427EMD2011S20
00810019242410EMD2010S40
00810019242403EMD2010S20
00810019242397EMD2008S40
00810019242380EMD2008S20

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