VERDENT LTD.

FDA Device Registration & Listing · LODZ Lodzkie, PL · Registration 3012628066

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
3012628066
FEI Number
3012628066
Entity Name
VERDENT LTD.
City/State/Country
LODZ Lodzkie, PL
Establishment Address
138 Lodowa str., LODZ Lodzkie 93-232, PL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Verdent Ltd. (Owner Number: 10052364)
Owner / Operator Contact Address
138 Lodowa str., Lodz, PL-10 93-232, PL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Verdent Verdent endodontic instruments Verdent Verdent dental instruments

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2020-07-20
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 2016-07-20
EKS File, Pulp Canal, Endodontic Dental Class 1 872.4565 2025-12-18
EJL Bur, Dental Dental Class 1 872.3240 2016-07-20
EIY Instrument, Filling, Plastic, Dental Dental Class 1 872.4565 2025-12-18

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Verdent Ltd.
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
K201622 Guangdong Kingfa Sci. & Tech.Co., Ltd. Medical surgical mask 2020-11-24
K881618 3M Company ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK 1988-05-09
K864976 Endo Technic Corp. SOLUSET CALCIUM DEMINERALIZING SOLUTION 1987-02-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012628066. Last updated year: 2026. Please use registration number 3012628066 when referencing this establishment in official correspondence.
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