Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010931810

FEI Number

3010931810

Entity Name

CREDENTIS AG

City/State/Country

Zug, CH

Establishment Address

Gubelstrasse 24, Zug 6300, CH

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

credentis ag (Owner Number: 10057783)

Owner / Operator Contact Address

Gubelstrasse 24, Zug, CH-ZG 6300, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PVA pad

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXR	Applicator, Resin	Dental	Class 1	872.3140	2024-04-16

Official Correspondent

Lucie Fischer

US Agent Details

Rebeca Santiago Business: vVardis Inc Email: rebeca.santiago@vvardis.com Phone: (856) 8788908

Related Public Records

Same Entity

credentis ag

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3026760	JORDCO, INC.	Hillsboro, OR, US
3016447764	DSI DENTAL SOLUTIONS LTD	Ashdod Southern, IL
3015272949	Ormco Corporation	Brea, CA, US
3008370577	SHANGHAI SMEDENT MEDICAL INSTRUMENT CO., LTD	Shanghai, CN
3009420946	HUANGHUA PROMISEE DENTAL CO., LTD	Huanghua Hebei, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010931810. Last updated year: 2026. Please use registration number 3010931810 when referencing this establishment in official correspondence.