Data / Medical devices / United States / Nature Major Inc.

Nature Major Inc.: FDA-registered device maker in Mineola, NY, United States, 7 510(k) clearances

Name: Nature Major Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Nature Major Inc. is registered with the FDA (registration 3014774380) in Mineola, NY, United States. It lists 8 device types. The FDA files 7 510(k) clearances under its listings, the newest dated September 21, 2020. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3014774380
Address: 300 Old Country Rd Ste Gl11, Mineola, NY, United States, 11501
Owner or operator: Nature Major Inc (10059908)
Roles: Repackager or relabeler
First device listed: May 21, 2019
Registered through: 2027
Brand names listed: Alcedo

Devices it lists

Device	Product code	Class	Role	Source
Container, Sharps	MMK	2	Repackager or relabeler	accessdata.fda.gov
Continuous Measurement Thermometer	FLL	2	Repackager or relabeler	accessdata.fda.gov
Oximeter	DQA	2	Repackager or relabeler	accessdata.fda.gov
Stimulator, Muscle, Powered	IPF	2	Repackager or relabeler	accessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle Conditioning	NGX	2	Repackager or relabeler	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain Relief	GZJ	2	Repackager or relabeler	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-Counter	NUH	2	Repackager or relabeler	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
September 21, 2020	K201467	Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B	DXN	Substantially Equivalent	Bioland Technology, Ltd.	accessdata.fda.gov
June 25, 2020	K200437	Blood Pressure Monitor	DXN	Substantially Equivalent	Shenzhen Jamr Technology Co., Ltd.	accessdata.fda.gov
November 1, 2019	K192087	Combo Electrotherapy Device	NUH	Substantially Equivalent	Shenzhen Roundwhale Technology Co. , Ltd.	accessdata.fda.gov
January 3, 2019	K180984	Maxcon Sharps Container	MMK	Substantially Equivalent	Ningbo Maxcon Medical Technology Co., Ltd.	accessdata.fda.gov
March 27, 2018	K170605	Upper Arm Type Electronic Blood Pressure Monitor Series, Electronic Blood Pressure Monitor: YE650A, YE650D, YE660B, YE670A and YE670D	DXN	Substantially Equivalent	Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.	accessdata.fda.gov
March 14, 2018	K172795	Infrared Thermometer	FLL	Substantially Equivalent	Shenzhen Jumper Medical Equipment Co., Ltd.	accessdata.fda.gov
August 28, 2014	K140582	FINGERTIP PULSE OXIMETER	DQA	Substantially Equivalent	Shenzhen Jumper Medical Equipment Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated September 21, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.