ADVANCED MEDTECH CORPORATE PTE LTD

FDA Device Registration & Listing · Singapore Central Singapore, SG · Registration 3016881508

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
3016881508
FEI Number
3016881508
Entity Name
ADVANCED MEDTECH CORPORATE PTE LTD
City/State/Country
Singapore Central Singapore, SG
Establishment Address
2 Venture Drive #23-18 Vision Exchange, Singapore Central Singapore 608526, SG
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Advanced MedTech Corporate Pte Ltd (Owner Number: 10073211)
Owner / Operator Contact Address
2 Venture Drive #23-18 Vision Exchange, Singapore, SG-NOTA 608526, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K243820
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FGB Ureteroscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2022-10-17
FGB Ureteroscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2020-05-07
FGB Ureteroscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2020-08-28
FAJ Cystoscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2022-11-21
FED Endoscopic Access Overtube, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2025-02-13

Official Correspondent

No official correspondent registered.

US Agent Details

John Hoffer Business: dornier medtech america inc Email: jhoffer@dornier.com Phone: (770) 5146163

Related Public Records

Same Entity

Advanced MedTech Corporate Pte 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
K915458 Psi Medical Products, Inc. URETEROSCOPE 1992-01-30
K230752 FUJIFILM Healthcare Americas Corporation Over-tube (TR-1208A); Over-tube (TR-1504A); Over-tube (TR-1507A) 2023-09-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016881508. Last updated year: 2026. Please use registration number 3016881508 when referencing this establishment in official correspondence.
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