Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017065670

FEI Number

3017065670

Entity Name

DERMAQUAL

City/State/Country

Johnson City, TN, US

Establishment Address

153 Cedar Grove Rd, Johnson City, TN 37601, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Dermaqual (Owner Number: 10075699)

Owner / Operator Contact Address

153 Cedar Grove rd, Johnson City, TN 37601, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bioginix Bioginix Centrifuge

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ORG	Platelet And Plasma Separator For Bone Graft Handling	Hematology	Class 2	864.9245	2021-07-15
GKG	Centrifuge, Hematocrit	Hematology	Class 2	864.6400	2023-12-08

Official Correspondent

Joseph Bawab

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dermaqual

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3015942805	JUVENTIX REGENERATIVE MEDICAL, LLC	Tampa, FL, US
3017364686	GALE FORCE AESTHETICS, LLC	Alamo, CA, US
1721676	Sterigenics U.S., LLC	Salt Lake City, UT, US
2183744	Isomedix Operations, Inc.	Minneapolis, MN, US
3009435759	ZIZION GROUP Inc.	Boca Raton, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017065670. Last updated year: 2026. Please use registration number 3017065670 when referencing this establishment in official correspondence.