Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1056339

FEI Number

1000140463

Entity Name

EAR TECHNOLOGY CORPORATION

City/State/Country

Johnson City, TN, US

Establishment Address

106 E Watauga Ave., Johnson City, TN 37601, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

EAR TECHNOLOGY CORPORATION (Owner Number: 9007312)

Owner / Operator Contact Address

106 East Watauga Ave., 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

Dry-Brik by Dry&Store Dry&Store Global II Dry Caddy by Dry&Store Zephyr by Dry&Store Breeze by Dry&Store Dry Disc by Dry&Store Dry Brik II DryBoost DryDome LightBeam Ear Curettes and Tweezers with Magnification Tweak Enhance OTC LightBeam Ear Curettes and Tweezers with Magnification Tweak Focus + T, Plaid, Tune Amp Focus + T Tweak Enhance OTC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ESD	Hearing Aid, Air-Conduction, Prescription	Ear, Nose, Throat	Class 1	874.3300	2007-12-13
LRC	Instrument, Ent Manual Surgical	Ear, Nose, Throat	Class 1	874.4420	2022-01-03
MEC	Disinfector, Medical Devices	General Hospital	Class 2	880.6992	2020-12-28
QUG	Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter	Ear, Nose, Throat	Class 2	874.3305	2023-06-20
JYG	Curette, Ear	Ear, Nose, Throat	Class 1	874.4420	1993-03-26
QUF	Hearing Aid, Air-Conduction, Over The Counter	Ear, Nose, Throat	Class 1	874.3300	2023-04-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EAR TECHNOLOGY CORPORATION

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
K892457	Telstar Electronics, Inc.	TELSTAR MODEL 1/3 ITE HEARING AID	1989-06-06
K760996	Unitron Industries, Inc.	HEARING AID (MODEL 695D, 905 & 960P)	1976-11-16
K840825	Maico Hearing Instruments, Inc.	SERIES MR IN-THE-EAR CUSTOM HEARING AID	1984-03-30
K946253	Maico Hearing Instruments, Inc.	MAICO IN-THE-EAR MODEL RD 201	1995-01-30
K863975	Gn Danavox, Inc.	CUSTOM IN-THE-EAR	1986-11-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0016-2026	Getinge Disinfection Ab Ljungadalsgatan	2	Getinge 88-Series Washer- Disinfector. Model Number: 88-5.
Z-0018-2014	Getinge Disinfection Ljungadalsgatan	2	Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in healthcare facilities where reusable items such as instruments, utensils, anesthesia sets, and glassware are handled for decontamination purposes.

Similar Registrations

Registration Number	Establishment Name	Location
3008713760	KENYON AUDIOLOGY	Bend, OR, US
3022507139	Zhongrui HearJoy Medical Equipment co., Ltd.	Shenzhen Guangdong, CN
3005785669	ALPS INTERNATIONAL	NEW DELHI, IN
2523819	MICROSONIC, INC.	AMBRIDGE, PA, US
3017618900	HUIZHOU GOLD ROSE TECHNOLOGY CO.,LTD	huizhou Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1056339. Last updated year: 2026. Please use registration number 1056339 when referencing this establishment in official correspondence.