VITASKY PRECISION TECHNOLOGY (THAILAND) CO., LTD.

FDA Device Registration & Listing · Bang Phli Samut Prakan, TH · Registration 3031754334

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
3031754334
FEI Number
3031754334
Entity Name
VITASKY PRECISION TECHNOLOGY (THAILAND) CO., LTD.
City/State/Country
Bang Phli Samut Prakan, TH
Establishment Address
888/9,10,6 Moo 21 Bang Phli Yai Subdistrict, Bang Phli Samut Prakan 10540, TH
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
VITASKY PRECISION TECHNOLOGY (THAILAND) CO., LTD. (Owner Number: 10091154)
Owner / Operator Contact Address
888/9,10,6 Moo 21 Bang Phli Yai Subdistrict, Bang Phli, TH-11 10540, TH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

snorkel diving mask Swimming Goggles fin

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZO Set, Tubing And Support, Ventilator (W Harness) Anesthesiology Class 1 868.5975 2024-07-14
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2024-07-14
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2024-07-14
ISH Component, External, Limb, Ankle/Foot Physical Medicine Class 1 890.3420 2024-07-14

Official Correspondent

Shelley wang

US Agent Details

Rebecca Toman Email: cs@ltlqa.com Phone: (281) 6008227

Related Public Records

Same Entity

VITASKY PRECISION TECHNOLOGY (THAILAND) CO., LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2026 Percussionaire Corporation 1
Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031754334. Last updated year: 2026. Please use registration number 3031754334 when referencing this establishment in official correspondence.
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