Sanbor Medical

FDA Device Registration & Listing · Allentown, PA, US · Registration 3007113169

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
3007113169
FEI Number
3007113169
Entity Name
Sanbor Medical
City/State/Country
Allentown, PA, US
Establishment Address
7584 Morris Court, Suite 218, Allentown, PA 18106, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Sanbor Medical (Owner Number: 10028522)
Owner / Operator Contact Address
7584 Morris Court, Suite 218, Allentown, PA 18106, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Spiro PD Personal Spirometer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZG Spirometer, Diagnostic Anesthesiology Class 2 868.1840 2016-02-22

Official Correspondent

Wayne Meng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sanbor 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
3007583504 Sanbor Medical Xiamen, Inc. Xiamen Fujian, CN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K923989 Sensor Medics Corp. SENSORMEDICS MODEL 6200 AUTOBOX DL 1993-08-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007113169. Last updated year: 2026. Please use registration number 3007113169 when referencing this establishment in official correspondence.
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