Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010812394

FEI Number

3010812394

Entity Name

DAAG MEDICAL INC

City/State/Country

Scottsdale, AZ, US

Establishment Address

9375 E Shea Blvd #100, Scottsdale, AZ 85260, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

DAAG Medical Inc (Owner Number: 10046458)

Owner / Operator Contact Address

9375 E Shea Blvd #100, Scottsdale, AZ 85260, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Thyroflex Percussor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GWZ	Percussor	Neurology	Class 1	882.1700	2014-03-24

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DAAG Medical Inc

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 3010812394. Last updated year: 2026. Please use registration number 3010812394 when referencing this establishment in official correspondence.