Data / Medical devices / Israel / Maya Medical Top Trade Ltd.
Maya Medical Top Trade Ltd.: FDA-registered device maker in Tsofit Central, Israel, 33 510(k) clearances
Maya Medical Top Trade Ltd. is registered with the FDA (registration 3036773433) in Tsofit Central, Israel. It lists 27 device types. The FDA files 33 510(k) clearances under its listings, the newest dated March 13, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3036773433
- Address
- Hashdera St. No. 54, Tsofit Central, Israel, 4492500
- Owner or operator
- Maya Medical Top Trade Ltd. (10092667)
- Roles
- Exporter to the US
- First device listed
- February 4, 2025
- Registered through
- 2027
- Brand names listed
- CERVICAL CUP GN VCARE PLUS, Hood, Flyte, Port&Palm Grip Obturator
Devices it lists
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 13, 2026 | K252040 | BD Vacutainer® Plasma Separator Tubes (PST), BD Vacutainer® Sodium Heparin Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 2, 2024 | K231373 | BD Vacutainer® K2 EDTA Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| December 20, 2023 | K230855 | BD Vacutainer® Serum Separator (SST) Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| September 20, 2023 | K230239 | AirSeal iFS System; AirSeal dV Solution | HIF | Substantially Equivalent | Conmed Corporation | accessdata.fda.gov |
| April 29, 2022 | K214045 | FreedomEdge Syringe Infusion System | FRN | Substantially Equivalent | Repro-Medical System, Inc., Dba Koru Medical Systems | accessdata.fda.gov |
| August 19, 2021 | K211104 | AirSeal® dV Solution- AirSeal® Cannula Cap and AirSeal® Bifurcated Filtered Tube Set | HIF | Substantially Equivalent | Conmed Corporation | accessdata.fda.gov |
| March 20, 2019 | K183399 | BD Nexiva Closed IV Catheter System | FOZ | Substantially Equivalent | Becton Dickinson Infusion Therapy Systems, Inc. | accessdata.fda.gov |
| October 23, 2018 | K180046 | Masimo Rad-97 and Accessories | DQA | Substantially Equivalent | Masimo Corporation | accessdata.fda.gov |
| September 11, 2018 | K173822 | Anchor Tissue Retrieval System by CONMED | GCJ | Substantially Equivalent | Conmed Corporation | accessdata.fda.gov |
| January 6, 2017 | K161463 | SureClip(TM) Repositionable Hemostasis Clip | PKL | Substantially Equivalent | Micro-Tech (Nanjing) Co., Ltd. | accessdata.fda.gov |
| December 19, 2016 | K162081 | BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin Syringe | FMF | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| June 10, 2015 | K150569 | LaparoVue | GCJ | Substantially Equivalent | Buffalo Filter, LLC | accessdata.fda.gov |
| March 20, 2015 | K143404 | SurgiQuest AirSeal iFS System | HIF | Substantially Equivalent | Surgiquest, Inc. | accessdata.fda.gov |
| February 10, 2015 | K142716 | VCARE | LKF | Substantially Equivalent | Conmed Corporation | accessdata.fda.gov |
| October 21, 2010 | K101896 | MASIMO LNCS/M-LNCS OXIMETRY SENSORS | DQA | Substantially Equivalent | Masimo Corporation | accessdata.fda.gov |
| October 5, 2007 | K071907 | VCARE RETRACTOR/ELEVATOR | LKF | Substantially Equivalent | Conmed Corporation | accessdata.fda.gov |
| March 23, 2007 | K063005 | STRYKER T6 HOODS AND TOGAS | FYA | Substantially Equivalent | Stryker Instruments | accessdata.fda.gov |
| December 10, 2004 | K043114 | KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE | KNT | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| May 14, 2004 | K041071 | BD VACUTAINER TRACE ELEMENT SERUM PLUS TUBE AND BD VACUTAINER TRACE ELEMENT K2EDTA PLUS TUBE, MODELS 368380/368381 | JKA | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
| January 16, 2004 | K032303 | STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM | HBE | Substantially Equivalent | Stryker Instruments | accessdata.fda.gov |
| March 26, 2003 | K024240 | BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS | JSM | Substantially Equivalent | Bd | accessdata.fda.gov |
| October 20, 1999 | K993138 | BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT | KNT | Substantially Equivalent | Ballard Medical Products | accessdata.fda.gov |
| August 11, 1999 | K983333 | BUFFALO FILTER VIROSAFE HRF- #VSHRFO1 | FYD | Substantially Equivalent | Buffalo Filter Co., Inc. | accessdata.fda.gov |
| July 28, 1999 | K991702 | MICROTAINER BRAND CHEMISTRY TUBES WITH MICROGARD CLOSURE, MODEL 365965, 365985, 365963, 365967, 36578 | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| September 13, 1996 | K963088 | SHEATH, ELECTROSURGICAL PENCIL | GEI | Substantially Equivalent | Aspen Laboratories, Inc. | accessdata.fda.gov |
| March 29, 1996 | K960250 | VACUTAINER BRAND PLUS SERUM & SST TUBES | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| November 28, 1995 | K954592 | VACUTAINER BRAND PST PLASMA SEPARATION TUBE | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| July 7, 1995 | K943227 | BUFFALO FILTER REPLACEMENT FILTER #BSUCF03 | FYD | Substantially Equivalent | Buffalo Filter Co., Inc. | accessdata.fda.gov |
| December 22, 1994 | K944681 | LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES | GEI | Substantially Equivalent | Birtcher Medical Systems, Inc. | accessdata.fda.gov |
| May 18, 1994 | K933652 | FREEDOM 60 SYRINGE INFUSION PUMP SYSTEM WITH SYRINGE SET & TUBING | FRN | Substantially Equivalent - Subject to Tracking Reg. | Repro-Med Systems, Inc. | accessdata.fda.gov |
| October 29, 1993 | K930059 | BUFFALO FILTER REPLACEMENT FILTER #BSTM300 | FYD | Substantially Equivalent | Buffalo Filter Co., Inc. | accessdata.fda.gov |
| February 19, 1991 | K904240 | SINGLE USE LAPARSCOPIC ELECTRODE | HFG | Substantially Equivalent | Aspen Labs | accessdata.fda.gov |
| April 4, 1979 | K790366 | URINE CULTURE KIT | JTW | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
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Updated March 13, 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.