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Data / Medical devices / Singapore / Pasture Pharma Pte Ltd

Pasture Pharma Pte Ltd: FDA-registered device maker in Corporation Place Central Singapore, Singapore, 3 510(k) clearances

Pasture Pharma Pte Ltd is registered with the FDA (registration 3006942307) in Corporation Place Central Singapore, Singapore. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 28, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3006942307
Address
2 Corporation Rd #03-04/05, Corporation Place Central Singapore, Singapore, 618494
Owner or operator
Pasture Pharma Pte Ltd (10024457)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
February 25, 2009
Registered through
2026
Brand names listed
Pasture 3 Ply Medimask, Pasture 60S Surgical Mask, Pasture A520G & Pasture 550G, Pasture PM10 N95, Pasture PM15 N95 and Pasture PM15s N595 Masks, Respirators

Devices it lists

DeviceProduct codeClassRoleSource
Mask, SurgicalFXX2Contract manufacturer, Manufactureraccessdata.fda.gov
Respirator, N95, For Use By The General Public In Public Health Medical EmergenciesNZJ2Exporter to the US, Manufactureraccessdata.fda.gov
Respirator, SurgicalMSH2Contract manufacturer, Exporter to the US, 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
October 28, 2015K141876Pasture F550S Surgical N95 Respirator, Pasture F550CS Surgical N95 Respirator, Pasture A520S Surgical N95 Respirator, Pasture A520CS Surgical N95 Respirator, Pasture E520S Surgical N95 Respirator, Pasture E520CS Surgical N95 RespiratorMSHSubstantially EquivalentPasture Pharma Pte, Ltd.accessdata.fda.gov
May 5, 2015K141875Pasture 60S Surgical MaskFXXSubstantially EquivalentPasture Pharma Pte, Ltd.accessdata.fda.gov
January 23, 2009K083176PASTURE, MODELS: F550, A520NZJSubstantially EquivalentPasture Pharma Pte, Ltd.accessdata.fda.gov

Compare with other makers

Updated October 28, 2015. 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.