ESRO AG

FDA Device Registration & Listing · Kilchberg Zurich, CH · Registration 3007345409

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
3007345409
FEI Number
3007345409
Entity Name
ESRO AG
City/State/Country
Kilchberg Zurich, CH
Establishment Address
Dorfstrasse 143, Kilchberg Zurich 8802, CH
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Esro AG (Owner Number: 10044230)
Owner / Operator Contact Address
Dorfstrasse 143, Kilchberg, CH-ZH 8802, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

paro glide-tape paro riser-floss paro travel-floss paro classic-floss paro brush'n floss paro 3star grip paro exS39 paro interspace brush F paro junior paro S39 paro M39 paro M27 paro flexi grip paro Isola Long paro medic paro superbrush paro flossholder paro isola F paroS43 paro ortho brush paro M43 paro baby paro S27 paro denture brush paro surgical brush paro M27L paro S27L

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JES Floss, Dental Dental Class 1 872.6390 2013-05-15
EFW Toothbrush, Manual Dental Class 1 872.6855 2013-05-15

Official Correspondent

Patrick Sutter

US Agent Details

Ofir Malka Business: Yourdent USA Email: om@yourdent-usa.com Phone: (646) 3204310

Related Public Records

Same Entity

Esro AG
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
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007345409. Last updated year: 2026. Please use registration number 3007345409 when referencing this establishment in official correspondence.
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