BELMED, INC.

FDA Device Registration & Listing · RED LION, PA, US · Registration 1119231

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
1119231
FEI Number
1119231
Entity Name
BELMED, INC.
City/State/Country
RED LION, PA, US
Establishment Address
887 DELTA RD., RED LION, PA 17356, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Sterilize Medical Device for Another Party (Contract Sterilizer),Remanufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Device in the United States for Export Only,Manufacture Medical Device for Another Party (Contract Manufacturer),Reprocess Single-Use Device,Manufacture Medical Device
Owner / Operator
BELMED, INC. (Owner Number: 1119231)
Owner / Operator Contact Address
887 DELTA RD., --, Red Lion, PA 17356, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

YOKE ASSEMBLY, MEDICAL GAS Flowmeter, tube, thorpe, back-pressure compensated

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAM Yoke Assembly, Medical Gas Anesthesiology Class 1 868.6885 1992-08-25
CAX Flowmeter, Tube, Thorpe, Back-Pressure Compensated Anesthesiology Class 1 868.2340 2015-05-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BELMED, INC.
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
K780365 Spica, Inc. OXYGEN/NITROUS OXIDE OUTLET 1978-03-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1119231. Last updated year: 2026. Please use registration number 1119231 when referencing this establishment in official correspondence.
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