MEDI-DOSE, INC.

FDA Device Registration & Listing · Warminster, PA, US · Registration 2521373

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
2521373
FEI Number
2521373
Entity Name
MEDI-DOSE, INC.
City/State/Country
Warminster, PA, US
Establishment Address
70 INDUSTRIAL DRIVE, Warminster, PA 18974, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
MEDI-DOSE, INC. (Owner Number: 2521373)
Owner / Operator Contact Address
70 INDUSTRIAL DRIVE, --, Warminster, PA 18974, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AUTOSQUEEZE AUTODROP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KCM Dropper, Ent Ear, Nose, Throat Class 1 874.5220 1995-01-31

Official Correspondent

ROBERT BRAVERMAN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEDI-DOSE, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2521373. Last updated year: 2026. Please use registration number 2521373 when referencing this establishment in official correspondence.
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