Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1226711

FEI Number

3003338236

Entity Name

TARRY MEDICAL PRODUCTS, INC.

City/State/Country

DANBURY, CT, US

Establishment Address

22 SHELTER ROCK LANE, DANBURY, CT 06810, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

TARRY MEDICAL PRODUCTS, INC. (Owner Number: 9044769)

Owner / Operator Contact Address

22 SHELTER ROCK LANE, --, Danbury, CT 06810, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TARRY BOARD TARRY ARM BOARD SLEEVES TARRY ARM BOARD DandlePURE NeoBellyBand Tarry Medical Temperature Probes Dandlelion Crown Cradle DANDLELION GEL PILLOWS TARRY GELS DONUTS MMS-ET1

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOD	Board, Arm (With Cover), Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2007-08-20
IKY	Mattress, Flotation Therapy, Non-Powered	General Hospital	Class 1	880.5150	2007-08-20
MDR	Binder, Medical, Therapeutic	General Hospital	Class 1	880.5160	2024-01-12
FMT	Warmer, Infant Radiant	General Hospital	Class 2	880.5130	2008-10-16
FMZ	Incubator, Neonatal	General Hospital	Class 2	880.5400	2008-10-16
MRI	Orthosis, Truncal/Orthosis, Limb	Physical Medicine	Class 1	890.3490	2018-10-12
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2007-08-20
JAY	Support, Breathing Tube	Anesthesiology	Class 1	868.5280	2010-06-01

Official Correspondent

Mandi Lowe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TARRY MEDICAL PRODUCTS, INC.

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
K020219	Replacement Parts Industries, Inc.	RPI SKIN OR AIR TEMPERATURE PROBE	2002-04-12
K881713	Gempco, Inc.	SPECIAL PROCEDURES BASE UNIT MODEL 500	1988-07-12
K943360	Ohmeda Medical	OHIO CARE PLUS INCUBATOR	1994-09-29

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0041-2020	Ohmeda Medical	2	Giraffe Omnibed - Product Usage: The OmniBed is a combination of an infant incubator and an infant warmer. The device can be operated as an incubator or as a warmer and can transition from one mode to the other on user s demand. It cannot be operated in both modes at the same time. Incubators and warmers provide heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Incubators provide an enclosed, temperature-controlled environment and warmers provide infrared heat in an open environment. They may also be used for short periods of time to facilitate the neonate s transition from the uterus to the external environment. This device may incorporate a Servo Controlled Oxygen Delivery System. This is indicated to provide stable oxygen concentration within the infant compartment at the value set by the operator (21-65%).

Similar Registrations

Registration Number	Establishment Name	Location
3008950799	JOEANNE DOMINICANA DIVISION OF JOEANNE COMPANY INTERNATIONAL	Santiago, DO
3010359088	LINGXIAN DONGSHENG TEXTILE CO., LTD.	Dezhou Shandong, CN
3008494300	Shaoxing Songqiao Textile Co, ltd	Shaoxing Zhejiang, CN
1218386	ALIMED, LLC	DEDHAM, MA, US
3011859755	Brady (Xiamen) Co. Ltd.	Xiamen Fujian, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1226711. Last updated year: 2026. Please use registration number 1226711 when referencing this establishment in official correspondence.