GROWTH-SONIC LIMITED

FDA Device Registration & Listing · KOWLOON, HK · Registration 3005951243

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
3005951243
FEI Number
3005951243
Entity Name
GROWTH-SONIC LIMITED
City/State/Country
KOWLOON, HK
Establishment Address
1829-1835 STAR HOUSE, 3 SALISBURY ROAD, TST, KOWLOON N/A, HK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
GROWTH-SONIC LIMITED (Owner Number: 10049328)
Owner / Operator Contact Address
1829-1835 STAR HOUSE, 3 SALISBURY ROAD, TST, KOWLOON, HK-NOTA 00000, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Hit promotional products Inc. Hit promotional products Inc. Hit Promotional Inc. Hit promotional products Inc. Hit promotional products Inc. Hit Promotional Inc. Hit promotional products Inc.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2015-05-12
EFW Toothbrush, Manual Dental Class 1 872.6855 2015-07-07
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2015-05-12
OVR Kit, First Aid, Talking General, Plastic Surgery Class 1 878.4014 2019-02-27
LKB Pad, Alcohol, Device Disinfectant Unknown Class U N/A 2015-06-12
PCM Portable Liquid Oxygen Unit Stand Physical Medicine Class 1 890.5050 2023-09-12
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2015-11-22

Official Correspondent

KWOK HO DAVID LEE

US Agent Details

Nancy Barahona Email: nbarahona@hitpromo.net Phone: (800) 2376035

Related Public Records

Same Entity

GROWTH-SONIC LIMITED
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005951243. Last updated year: 2026. Please use registration number 3005951243 when referencing this establishment in official correspondence.
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