VENNER MEDICAL (SINGAPORE) PTE LTD

FDA Device Registration & Listing · Singapore Central Singapore, SG · Registration 3007740622

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007740622
FEI Number
3007740622
Entity Name
VENNER MEDICAL (SINGAPORE) PTE LTD
City/State/Country
Singapore Central Singapore, SG
Establishment Address
35 Joo Koon Circle, Singapore Central Singapore 629110, SG
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Venner Medical (Singapore) Pte Ltd (Owner Number: 10029896)
Owner / Operator Contact Address
35 Joo Koon Circle, Singapore, SG-05 629110, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BYX Tubing, Pressure And Accessories Anesthesiology Class 1 868.5860 2012-08-29
BTR Tube, Tracheal (W/Wo Connector) Anesthesiology Class 2 868.5730 2010-05-13
BSK Cuff, Tracheal Tube, Inflatable Anesthesiology Class 2 868.5750 2011-09-12

Official Correspondent

No official correspondent registered.

US Agent Details

Christine L. Brauer Brauer Business: Brauer Device Consultants, LLC Email: chris.brauer@comcast.net Phone: (301) 5451990

Related Public Records

Same Entity

Venner Medical (Singapore) Pte Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K233341 Covidien, LLC Shiley™ Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440, 87445, 87450, 87455, 87460, 87465, 87470, 87475, 87480, 87485, 87490, 87495, 87410) 2024-05-20
K243785 Covidien, LLC Shiley™ Oral/Nasal Tracheal Tube with TaperGuard™ Cuff Reinforced, Murphy Eye Shiley™ Tracheal Tube TaperGuard™ Cuff Reinforced with Stylet Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced, Murphy Eye Shiley™ Oral/Nasal Tracheal Tube Cuffless Reinforced 2025-09-25

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-2014 H & H Associates 2
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, labeled in part ***H & H Associates, Inc. CAGE 1NNH6 www.gohandh.com Ordinary, VA 23131 (800) 326-5708***. The product is used to maintain fracture alignment.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007740622. Last updated year: 2026. Please use registration number 3007740622 when referencing this establishment in official correspondence.
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