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Data / Medical devices / United Arab Emirates / Nas Med LLC FZ

Nas Med LLC FZ: FDA-registered device maker in DUBAI Dubayy, United Arab Emirates, 25 510(k) clearances and 4 PMA approvals

Nas Med LLC FZ is registered with the FDA (registration 3035387162) in DUBAI Dubayy, United Arab Emirates. It lists 19 device types. The FDA files 25 510(k) clearances and 4 PMA approvals under its listings, the newest dated January 12, 2024. Registered through 2026. FDA data exported November 3, 2026.

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Get makers like this oneWatch Nas Med LLC FZ
FDA registration number
3035387162
Address
Business Center 1 M Floor The Medan Hotel Nad Al Sheba, DUBAI Dubayy, United Arab Emirates, 00000
Owner or operator
NAS MED LLC FZ (10092611)
Roles
Exporter to the US
First device listed
January 27, 2025
Registered through
2026
Brand names listed
3D MAX MESH, ABSORBABLE FIXATION DEVICE, ABSORBABLE GHEMOSTAT, CDH29B, CLIPS, DURAGEN, DURASEAL, ENDOGIA and more

Devices it lists

DeviceProduct codeClassRoleSource
Absorbable Collagen Hemostatic Agent With ThrombinPMX3Exporter to the USaccessdata.fda.gov
Agent, Absorbable Hemostatic, Collagen BasedLMF3Exporter to the USaccessdata.fda.gov
Agent, Absorbable Hemostatic, Non-Collagen BasedLMG3Exporter to the USaccessdata.fda.gov
Barrier, Absorbable, AdhesionMCN3Exporter to the USaccessdata.fda.gov
Clip, ImplantableFZP2Exporter to the USaccessdata.fda.gov
Colposcope (And Colpomicroscope)HEX2Exporter to the USaccessdata.fda.gov
Dura SubstituteGXQ2Exporter to the USaccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Exporter to the USaccessdata.fda.gov
Endoscopic Tissue Approximation DeviceOCW2Exporter to the USaccessdata.fda.gov
Hysteroscope (And Accessories)HIH2Exporter to the USaccessdata.fda.gov
Instrument, Ultrasonic SurgicalLFLUExporter to the USaccessdata.fda.gov
Laparoscope, General & Plastic Surgery, ReprocessedNLM2Exporter to the USaccessdata.fda.gov
Mesh, Surgical, PolymericFTL2Exporter to the USaccessdata.fda.gov
Needle, Hypodermic, Single LumenFMI2Exporter to the USaccessdata.fda.gov
Sealant, DuralNQR3Exporter to the USaccessdata.fda.gov
Staple, ImplantableGDW2Exporter to the USaccessdata.fda.gov
Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac TissueOCL2Exporter to the USaccessdata.fda.gov
Suture, Nonabsorbable, Synthetic, PolypropyleneGAW2Exporter to the USaccessdata.fda.gov
System, Surgical, Computer Controlled InstrumentNAY2Exporter to the USaccessdata.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
January 12, 2024K232970Hem-o-lok® Ligating ClipsFZPSubstantially EquivalentTeleflex Medicalaccessdata.fda.gov
November 1, 2023K233402Bard 3DMax MeshFTLSubstantially EquivalentDavol Inc., Subsidiary of C. R. Bard, Inc.accessdata.fda.gov
August 29, 2023K232313LIGACLIP Endoscopic Rotating Multiple Clip Applier 12mm L (ER420); LIGACLIP Endoscopic Rotating Multiple Clip Applier 10mm M/L (ER320)FZPSubstantially EquivalentEthicon Endo Surgery, LLCaccessdata.fda.gov
March 23, 2021K202917LigaSure Exact Dissector, Nano-coatedGEISubstantially EquivalentCovidien, LLCaccessdata.fda.gov
December 19, 2018K182610Valleylab FT10 Electrosurgical Platform, Cardioblate BP2 Surgical Ablation Device, Cardioblate LP Surgical Ablation DeviceOCLSubstantially EquivalentMedtronicaccessdata.fda.gov
November 9, 2018K180395EZ-IO Intraosseous Vascular Access SystemFMISubstantially EquivalentArrow International, Inc. (Subsidiary of Teleflex, Inc.)accessdata.fda.gov
July 5, 2018K173721SureForm 60 and SureForm 60 ReloadsNAYSubstantially EquivalentIntuitive Surgicalaccessdata.fda.gov
May 8, 2018K173901MyoSure MANUAL Tissue Removal DeviceHIHSubstantially EquivalentHologic, Inc.accessdata.fda.gov
May 21, 2017K170446LT-300 SD Digital Video ColposcopeHEXSubstantially EquivalentLutech Industries, Inc.accessdata.fda.gov
April 21, 2017K170869LigaSure Maryland Jaw Sealer/Divider One-step Sealing, Nano-coatedGEISubstantially EquivalentCovidienaccessdata.fda.gov
April 18, 2017K163523ECHELON CIRCULAR Powered StaplerGDWSubstantially EquivalentEthicon Endo-Surgery, LLCaccessdata.fda.gov
November 14, 2016K162941Ligasure Blunt Tip, Sealer/Divider, Nano-coatedGEISubstantially EquivalentCovidienaccessdata.fda.gov
September 15, 2016K162047LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coatedGEISubstantially EquivalentCovidienaccessdata.fda.gov
April 26, 2016K160176Signia StaplerGDWSubstantially EquivalentCovidienaccessdata.fda.gov
December 19, 2014K142777Weck Hem-o-lok Auto Endo5 Ligating Clip ApplierFZPSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
December 3, 2013K132974AQUAMANTYS 2.3 BIPOLAR SEALER, EVS 4.0 EPIDURAL VEIN SEALER, MINI EVS 3.4 EPIDURAL VEIN SEALER, SBS 5.0 SHEATHED BIPOLARGEISubstantially EquivalentMedtronic Advanced Energy, LLCaccessdata.fda.gov
August 22, 2012K121550HARMONIC ACE LAPAROSCOPIC 5MM DIAMETER SHEARS 36CM LENGTH + ADAPTIVE TISSUE TECHNOLOGYLFLSubstantially EquivalentEthicon Endo-Surgery, LLCaccessdata.fda.gov
October 25, 2011K111825ENDO GIA(TM) STAPLERS, DST SERIES(TM) GIA(TM) STAPLERS, DST SERIES(TM) TA(TM) STAPLERSGDWSubstantially EquivalentCovidien, Formerly US Surgical A Divison of Tyco Haccessdata.fda.gov
April 7, 2010K093845ETHICON SECURESTRAP 5MM ABSORBABLE STRAP FIXATION DEVICE, MODEL STRAP25GDWSubstantially EquivalentETHICON, Inc.accessdata.fda.gov
March 19, 2010K100080REPROCESSED TROCARS, MODEL B5LT AND CB5LTNLMSubstantially EquivalentAscent Healthcare Solutionsaccessdata.fda.gov
May 14, 2009K090470AUTOSUTURE PROTACK; TACKER SYSTEM; ABSORBATACK FIXATION DEVICESOCWSubstantially EquivalentCovidienaccessdata.fda.gov
June 1, 2005K050947MODIFICATION TO: MODIFIED USS POLYPROPYLENE SUTUREGAWSubstantially EquivalentUnited States Surgical, A Division of Tyco Healthcaccessdata.fda.gov
September 30, 2003K032693DURAGEN PLUS DURAL GRAFT MATRIXGXQSubstantially EquivalentIntegra Lifesciences Corp.accessdata.fda.gov
August 14, 2002K021808WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIERFZPSubstantially EquivalentWeckaccessdata.fda.gov
December 18, 1998K983536PROXIMATE CURVED AND STRAIGHT INTRALUMINAL STAPLERSGDWSubstantially EquivalentEthicon Endo-Surgery, Inc.accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
April 7, 2005P040034DURASEAL DURAL SEALANT SYSTEMNQR38February 27, 2026accessdata.fda.gov
December 8, 1999P990009FLOSEAL MATRIX/FLOSEAL MATRIX HEMOSTATIC SEALANT/PROCEED HEMOSTATIC SEALANTPMX74November 13, 2025accessdata.fda.gov
September 15, 1989P880047INTERCEED TC7 ABSORBABLE ADHESION BARRIERMCN65June 25, 2026accessdata.fda.gov
October 14, 1960N12159SURGICEL BRAND ABSORBABLE HEMOSTATLMG120July 28, 2026accessdata.fda.gov

Compare with other makers

Updated February 27, 2026. 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.