Nature Major Inc.

FDA Device Registration & Listing · Mineola, NY, US · Registration 3014774380

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
3014774380
FEI Number
3014774380
Entity Name
Nature Major Inc.
City/State/Country
Mineola, NY, US
Establishment Address
300 Old Country Rd Ste Gl11, Mineola, NY 11501, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Nature Major Inc (Owner Number: 10059908)
Owner / Operator Contact Address
300 Old Country Rd Ste GL11, Mineola, NY 11501, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K172795
PMA Number
N/A

All Registered Proprietary Names

Alcedo

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMK Container, Sharps General Hospital Class 2 880.5570 2019-05-21
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2021-07-15
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2020-07-30
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2020-07-30
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2020-07-30
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2020-07-30
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2025-09-15
DQA Oximeter Cardiovascular Class 2 870.2700 2020-07-30
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2019-10-18

Official Correspondent

Jianing Pu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nature Major Inc
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
K100940 Andon Health Co, Ltd. FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-5965 2010-06-29
K251581 Shenzhen Hingmed Medical Instrument Co., Ltd. Wearable Ambulatory Blood Pressure Monitor (WBP-02A) 2026-02-13
K200521 Health & Life Co., Ltd. Full Automatic(NIBP) Blood Pressure Monitor 2020-06-12
K152003 Andon Health Co, Ltd. iHealth BP3L Wireless Blood Pressure Monitor 2015-09-24
K952827 Sein Electronics Co., Ltd. FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 1996-11-14

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0032-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.
Z-0020-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014774380. Last updated year: 2026. Please use registration number 3014774380 when referencing this establishment in official correspondence.
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