ANCHOR PLUS/NEO ANCHOR PLUS

GUDID 08809488210114

KJMEDITECH.CO.,LTD

Orthodontic anchoring screw
Primary Device ID08809488210114
NIH Device Record Key8b4824c0-1ceb-42f3-b7b7-0e749fafcb4a
Commercial Distribution StatusIn Commercial Distribution
Brand NameANCHOR PLUS/NEO ANCHOR PLUS
Version Model NumberMS-1606
Company DUNS688476027
Company NameKJMEDITECH.CO.,LTD
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 Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108809488210114 [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 StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-01-03
Device Publish Date2019-08-26

On-Brand Devices [ANCHOR PLUS/NEO ANCHOR PLUS]

08809488210251MSS-1612
08809488210244MSS-1610
08809488210237MSS-1608
08809488210220MSS-1607
08809488210213MSS-1606
08809488210206MSS-1412
08809488210190MSS-1410
08809488210183MSS-1408
08809488210176MSS-1407
08809488210169MSS-1406
08809488210152MS-1612
08809488210145MS-1610
08809488210138MS-1608
08809488210121MS-1607
08809488210114MS-1606
08809488210107MS-1412
08809488210091MS-1410
08809488210084MS-1408
08809488210077MS-1407
08809488210060MS-1406

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