NOAH MEDICAL Corp.

FDA Device Registration & Listing · San Carlos, CA, US · Registration 3033628477

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
3033628477
FEI Number
3033628477
Entity Name
NOAH MEDICAL Corp.
City/State/Country
San Carlos, CA, US
Establishment Address
975 Industrial Rd, San Carlos, CA 94070, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Noah Medical (Owner Number: 10087546)
Owner / Operator Contact Address
2075 Zanker Rd., San Jose, CA 95131, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223144
PMA Number
N/A

All Registered Proprietary Names

Galaxy System Galaxy system bronchoscope and accessory kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EOQ Bronchoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4680 2023-03-13

Official Correspondent

Sam Mostafavi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3025749544 Tianjin Puli Ark Medical Technology Co., Ltd Dongli District Tianjin, CN
3027205723 NOAH MEDICAL Corp. Sunnyvale, CA, US
3021325287 NOAH MEDICAL Corp. San Jose, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K811059 Pentax Precision Instrument Corp. PENTAX BRONCHOFIBERSCOPE #FB-15A 1981-05-27
K142934 Covidien CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved 2015-06-17
K240075 FUJIFILM Healthcare Americas Corporation FUJIFILM Endoscope Model EB-710XT 2024-02-07

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0025-2020 AURIS HEALTH INC 2
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033628477. Last updated year: 2026. Please use registration number 3033628477 when referencing this establishment in official correspondence.
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