Medidenta

FDA Device Registration & Listing · Las Vegas, NV, US · Registration 1052939

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
1052939
FEI Number
1000113887
Entity Name
Medidenta
City/State/Country
Las Vegas, NV, US
Establishment Address
3575 W Post Rd, Las Vegas, NV 89118, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Medidenta (Owner Number: 10083326)
Owner / Operator Contact Address
3575 W Post Rd, Las Vegas, NV 89118, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Autoscaler Medi-Scaler

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ELC Scaler, Ultrasonic Dental Class 2 872.4850 2021-11-16

Official Correspondent

Alfred Perez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K832443 California Technics, Inc. ULTRASONIC DENTAL PROPHYLAXIS UNIT 1983-09-12
K994299 Bonart Co., Ltd. ART-P3, MODEL P3-1-ART-A1 2000-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1052939. Last updated year: 2026. Please use registration number 1052939 when referencing this establishment in official correspondence.
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