Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005024024

FEI Number

3005024024

Entity Name

GOLDEN SEASON PTE LTD

City/State/Country

SINGAPORE North West, SG

Establishment Address

31 Playfair Road, SINGAPORE North West 367993, SG

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

GOLDEN SEASON PTE LTD (Owner Number: 9070483)

Owner / Operator Contact Address

31 Playfair Road, SINGAPORE, SG-NOTA 367993, SG

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Trauma Shear Wheeled Litter Carrier NAR S-Rolled Gauze Raptor Restraint block MARK IV BED RAVEN R EVACUATION LITTER VARIOUS ACCE Quad Fold Stretcher TALON II R EVACUATION LITTER Multiple IV POLE OR STAND Emergency Dressing

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JOK	Scissors, Medical, Disposable	General Hospital	Class 1	880.6820	2010-07-13
FMR	Device, Transfer, Patient, Manual	General Hospital	Class 1	880.6785	2016-07-14
NAB	Gauze / Sponge,Nonresorbable For External Use	General, Plastic Surgery	Class 1	878.4014	2018-03-07
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2019-04-16
NZD	Stretcher, Patient Restraint	General Hospital	Class 1	880.6900	2022-07-22
FNJ	Bed, Manual	General Hospital	Class 1	880.5120	2007-12-12
FPP	Stretcher, Hand-Carried	General Hospital	Class 1	880.6900	2005-02-16
FOX	Stand, Infusion	General Hospital	Class 1	880.6990	2005-02-16
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2020-07-23

Official Correspondent

Noreen Ling

US Agent Details

William Slevin Business: Principal Email: qara@medapprovalllc.com Phone: (404) 5935005

Related Public Records

Same Entity

GOLDEN SEASON 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
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

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3038283966	L WELL MEDTECH SOLUTIONS SDN. BHD.	Nibong Tebal Pulau Pinang, MY
3012034017	Heaven Healthcare Co., Ltd.	Shaoxing Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005024024. Last updated year: 2026. Please use registration number 3005024024 when referencing this establishment in official correspondence.