Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2026894

FEI Number

2026894

Entity Name

THAYER MEDICAL CORPORTATION

City/State/Country

TUCSON, AZ, US

Establishment Address

4575 S PALO VERDE RD STE 337, TUCSON, AZ 85714, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

THAYER MEDICAL CORP. (Owner Number: 2026894)

Owner / Operator Contact Address

4575 S PALO VERDE RD STE 337, Tucson, AZ 85714, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K102658

PMA Number

N/A

All Registered Proprietary Names

MINISPACER® MDI ADAPTER WITH COUNTER INCREMENTING ACTUATOR 1024A 1543A 1025A QUAKE® VIBRATORY PEP DEVICE LiteAire Dual-Valved, Collapsible MDI Holding Chamber 1088 1009 VALVED TEE ADAPTER 1008 1085 LITEAIRE® COLLAPSIBLE VALVED HOLDING CHAMBER MINISPACER® DUAL-SPRAY MDI ADAPTER 1543 1025 1024

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CAF	Nebulizer (Direct Patient Interface)	Anesthesiology	Class 2	868.5630	2011-12-31
BYI	Percussor, Powered-Electric	Anesthesiology	Class 2	868.5665	2007-10-11
NVP	Holding Chambers, Direct Patient Interface	Anesthesiology	Class 2	868.5630	2022-12-22
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2008-06-20
NVP	Holding Chambers, Direct Patient Interface	Anesthesiology	Class 2	868.5630	2017-12-29
CAF	Nebulizer (Direct Patient Interface)	Anesthesiology	Class 2	868.5630	2010-12-16

Official Correspondent

James Strickland

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

THAYER MEDICAL CORP.

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
K163485	Adherium (Nz), Ltd.	SmartTouch	2017-08-30
K781467	Travenol Laboratories, S.A.	U-FLOAT VALVE 2D9023	1978-09-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2026	Percussionaire Corporation	1	Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

Similar Registrations

Registration Number	Establishment Name	Location
1110315	MYLAN PHARMACEUTICALS INC.	Morgantown, WV, US
3018783526	CEVA LOGISTICS NETHERLANDS BV (Venray)	Oostrum Limburgh, NL
3005998497	SUNMED AP, LTD.	ZHUHAI Guangdong, CN
3006852037	Omron Healthcare Manufacturing Vietnam Co., Ltd.	Ho Chi Minh City, VN
3006783791	GaleMed (Xiamen) Co., Ltd.	XIAMEN Fujian, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2026894. Last updated year: 2026. Please use registration number 2026894 when referencing this establishment in official correspondence.