K DENT GLOBAL

FDA Device Registration & Listing · Glendale, CA, US · Registration 3013543747

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013543747
FEI Number
3013543747
Entity Name
K DENT GLOBAL
City/State/Country
Glendale, CA, US
Establishment Address
616 E Glenoaks Blvd Ste 201, Glendale, CA 91207, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
K Dent Global (Owner Number: 10055430)
Owner / Operator Contact Address
251 W Dryden, Glendale, CA 91202, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K141421
PMA Number
N/A

All Registered Proprietary Names

Crown & Bridge

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBG Crown And Bridge, Temporary, Resin Dental Class 2 872.3770 2017-07-24

Official Correspondent

Karen Arakelyan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

K Dent Global
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013543747. Last updated year: 2026. Please use registration number 3013543747 when referencing this establishment in official correspondence.
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