Skip to the page

Data / Medical devices / Thailand / Thai Hospital Products Co., Ltd.

Thai Hospital Products Co., Ltd.: FDA-registered device maker in BANGPUD, PAKKRED, Nonthaburi, Thailand, 1 510(k) clearance

Thai Hospital Products Co., Ltd. is registered with the FDA (registration 9615909) in BANGPUD, PAKKRED, Nonthaburi, Thailand. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 29, 2011. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
9615909
FEI number
3003024808
Address
45/2, 45/3 Moo 2, Sukhaprachasun 2 Road, BANGPUD, PAKKRED, Nonthaburi, Thailand, 11120
Owner or operator
THAI HOSPITAL PRODUCTS CO., LTD. (9011535)
Roles
Contract manufacturer, Manufacturer
First device listed
September 29, 1994
Registered through
2026
Brand names listed
ACCESSORY, CAP, CONDUCTIVE, DISPOSABLE FACE MASK, DISPOSABLE SHOE COVER, SUIT, SURGICAL APPAREL, Surgical Mask

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Contract manufacturer, Manufactureraccessdata.fda.gov
Cap, SurgicalFYF1Contract manufacturer, Manufactureraccessdata.fda.gov
Cover, Shoe, Operating-RoomFXP1Contract manufacturer, Manufactureraccessdata.fda.gov
Mask, SurgicalFXX2Contract manufacturer, Manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Contract manufacturer, Manufactureraccessdata.fda.gov
Shoe And Shoe Cover, ConductiveBWP1Contract manufacturer, Manufactureraccessdata.fda.gov
Suit, SurgicalFXO1Contract manufacturer, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 29, 2011K110455KIMBERLY-CLARK LOW BARRIER, ASTM 2100 FACE MASKSFXXSubstantially EquivalentKimberly-Clark Corp.accessdata.fda.gov

Compare with other makers

Updated April 29, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.