SHENZHEN SANY PIONEER TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3016674860

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
3016674860
FEI Number
3016674860
Entity Name
SHENZHEN SANY PIONEER TECHNOLOGY CO., LTD.
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
503A, 302, No.2 Factory Building, Fukang Road,, Pinghu Community, Pinghu Street, Longgang District,, Shenzhen Guangdong 518000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen Sany Pioneer Technology Co.,Ltd (Owner Number: 10062741)
Owner / Operator Contact Address
503A, 302, No.2 Factory Building, Fukang Road, Pinghu Street, Longgang District, Shenzhen, CN-GD 518000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Snoring Mouth Guard L-size Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB) S-size Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB) Anti snoring mouthpiece (L09-T, L09-B) L07 Anti snoring mouthpiece Headgear Strap Headbands Headgear

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRK Device, Anti-Snoring Dental Class 2 872.5570 2026-03-09
LRK Device, Anti-Snoring Dental Class 2 872.5570 2025-11-17
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2025-11-17
BTK Strap, Head, Gas Mask Anesthesiology Class 1 868.5560 2022-01-10

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Shenzhen Sany Pioneer Technology Co.,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
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016674860. Last updated year: 2026. Please use registration number 3016674860 when referencing this establishment in official correspondence.
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