ESCALON MEDICAL CORP

FDA Device Registration & Listing · NEW BERLIN, WI, US · Registration 2183477

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
2183477
FEI Number
2183477
Entity Name
ESCALON MEDICAL CORP
City/State/Country
NEW BERLIN, WI, US
Establishment Address
2440 SOUTH 179TH ST., NEW BERLIN, WI 53146, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ESCALON MEDICAL CORP (Owner Number: 2183477)
Owner / Operator Contact Address
2440 SOUTH 179TH ST., --, New Berlin, WI 53146, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Universal Gas Mixing Kit Universal Viscous Fluid Control Pack BL7600

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXX Calibrator, Pressure, Gas Anesthesiology Class 1 868.2620 2016-01-14
MRH Pump, Infusion, Ophthalmic General Hospital Class 2 880.5725 2021-06-07

Official Correspondent

Denise Scheffler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ESCALON MEDICAL CORP
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183477. Last updated year: 2026. Please use registration number 2183477 when referencing this establishment in official correspondence.
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