Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2518153

FEI Number

2518153

Entity Name

DRUMMOND SCIENTIFIC CO.

City/State/Country

BROOMALL, PA, US

Establishment Address

500 PKWY., BROOMALL, PA 19008, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DRUMMOND SCIENTIFIC CO. (Owner Number: 2518153)

Owner / Operator Contact Address

500 PKWY., --, Broomall, PA 19008, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Microsafe; Safe-Cap Hematoclad

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GIO	Tube, Collection, Capillary Blood	Hematology	Class 1	864.6150	2023-11-10
GHY	Hematocrit, Tube, Rack, Sealer, Holder	Hematology	Class 2	864.6400	1992-07-29

Official Correspondent

Matt Herm

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DRUMMOND SCIENTIFIC CO.

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 2518153. Last updated year: 2026. Please use registration number 2518153 when referencing this establishment in official correspondence.