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Data / Medical devices / Malaysia / Molnlycke Health Care SDN BHD

Molnlycke Health Care SDN BHD: FDA-registered device maker in Kulim Kedah, Malaysia, 12 510(k) clearances

Molnlycke Health Care SDN BHD is registered with the FDA (registration 3025355668) in Kulim Kedah, Malaysia. It lists 1 device type. The FDA files 12 510(k) clearances under its listings, the newest dated May 24, 2019. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3025355668
Address
Lot 12A, Jalan Hi-Tech 7 Industrial Zone Phase 2, Kulim Hi-Tech Park, Kulim Kedah, Malaysia, 09090
Owner or operator
MOLNLYCKE HEALTH CARE US LLC (8030877)
Roles
Manufacturer
First device listed
May 7, 2008
Registered through
2026
Brand names listed
BIOGEL ECLIPSE, LATEX, POWDER FREE, INDICATOR UNDERGLOVE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS), Biogel Eclipse, Biogel Indicator Underglove, Biogel NeoDerm, Biogel Opti-Fit Ortho surgical gloves, Biogel PI Indicator, Biogel PI OrthoPro, Biogel PI Pro-Fit surgical glove and more

Devices it lists

DeviceProduct codeClassRoleSource
Surgeon'S GlovesKGO1Manufactureraccessdata.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
May 24, 2019K190077Biogel® PI UltraTouch S Surgical Glove, Biogel® Pl Ultra Touch S Indicator UndergloveKGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
September 20, 2011K112257BIOGEL PI ORTHOPRO BROWN SURGICAL GLOVEKGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
August 26, 2008K081180SKINSENSE POLYISOPRENE UNDERGLOVEKGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
September 11, 2007K071700BIOGEL SENSOR SURGEON'S GLOVE WITH NON-PYROGENIC STATEMENTKGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
September 11, 2007K071465BIOGEL ORTHOPAEDIC SURGICAL GLOVE WITH NON-PRYOGENIC STATEMENTKGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
September 10, 2007K071565BIOGEL INDICATOR UNDERGLOVE WITH NON-PYROGENIC STATEMENTKGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
September 10, 2007K071414BIOGEL ECLIPSE, LATEX, POWDER FREE, INDICATOR UNDERGLOVE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)KGOSubstantially EquivalentMolnlycke Health Care Us, LLCaccessdata.fda.gov
March 10, 2006K053102BIOGEL SKINSENSE POWDER-FREE NON-LATEX SURGEON'S GLOVEKGOSubstantially EquivalentRegent Medical Americas, LLCaccessdata.fda.gov
March 7, 2006K053442BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVEKGOSubstantially EquivalentRegent Medical Americas, LLCaccessdata.fda.gov
February 1, 2006K053443BIOGEL ECLIPSE NON-PYROGENIC LATEX POWDER-FREE STERILE SURGEON'S GLOVEKGOSubstantially EquivalentRegent Medical Americas, LLCaccessdata.fda.gov
March 16, 2005K050184BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVEKGOSubstantially EquivalentRegent Medical Americas, LLCaccessdata.fda.gov
August 14, 2000K000421BIOGEL NEOTECH II POWDER-FREE NEOPRENE SURGEON'S GLOVEKGOSubstantially EquivalentSsl Americas, Inc. (Regent Medical)accessdata.fda.gov

Compare with other makers

Updated May 24, 2019. 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.