InBody Co, Ltd.

FDA Device Registration & Listing · Cheonan-si Chungnam, KR · Registration 3003074886

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
3003074886
FEI Number
3003074886
Entity Name
InBody Co, Ltd.
City/State/Country
Cheonan-si Chungnam, KR
Establishment Address
15, Heugam-gil , Ipjang-myueon, Seoubuk-gu,, Cheonan-si Chungnam 31025, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
InBody Co. Ltd. (Owner Number: 9041413)
Owner / Operator Contact Address
15, Heugam-gil, Ipjang-myueon, Seoubuk-gu,, Cheonan-si,, KR-44 31025, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

IB-GAIT2 BP170B BPBIO250 BP160B BP170 BP160 Disposable Cuff Barrier LookinBody120 LookinBody 110 LookinBody Web LookinBody M20 Lookin'Body 110 InBody Touch InBody Touch 24i Scale BPBIO320n BPBIO320 BPBIO680KV BPBIO 320 S BPBIO780KV BPBIO 320 SN BPBIO 330 S BPBIO 330 SN BPBIO 750 InBody 270 InBody270 InBody R20B InBody R20 INBODY770 INBODY H20(B) InBody S10 INBODY H20 INBODY570 InBody Dial InBody Dial H20 InGrip(IB-HGSm) InGrip Handgrip Strength Dynamometer Yscope InBody BAND2 InBody970 BWA2 InBody380 InBody970S InBody770S InBody580 InBody270S BWA2S InBody280 BPBIO220T BPBIO210T BPBIO210 BPBIO220 Scale InBody370 InBody 720 InBody 520 InBody120 InBody120R InBody370S InBody230 InBody570 InBody770G InBody S10 InBody270 Inbody470 InBody H20B InBody 470 InBody 270 InBody M20 InBody 770 InBody 230 InBody970 BWA2 BWA ON InBody580 InBody380 InBody Tissue IB-LS BSM370

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISD Exerciser, Measuring Physical Medicine Class 2 890.5360 2026-05-26
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2020-12-04
OEA Non-Surgical Gown General, Plastic Surgery Class 1 878.4040 2021-04-14
OUG Medical Device Data System General Hospital Class 1 880.6310 2011-03-30
KHX Platform, Force-Measuring Physical Medicine Class 1 890.1575 2020-06-10
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2013-09-11
MNW Analyzer, Body Composition Cardiovascular Class 2 870.2770 2012-07-30
MNW Analyzer, Body Composition Cardiovascular Class 2 870.2770 2013-09-11
LBB Dynamometer, Ac-Powered Orthopedic Class 2 888.1240 2023-10-30
PUH Analyzer, Body Composition, Exempt Cardiovascular Class 2 870.2770 2020-02-25
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2021-01-06
DXQ Blood Pressure Cuff Cardiovascular Class 2 870.1120 2021-01-06
FRW Scale, Patient General Hospital Class 1 880.2720 2010-11-08
MNW Analyzer, Body Composition Cardiovascular Class 2 870.2770 2013-11-27
MNW Analyzer, Body Composition Cardiovascular Class 2 870.2770 2014-10-03
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2021-02-09
IKK System, Isokinetic Testing And Evaluation Physical Medicine Class 2 890.1925 2020-07-17
FRI Scale, Stand-On, Patient General Hospital Class 1 880.2700 2010-08-31

Official Correspondent

No official correspondent registered.

US Agent Details

Daniel Kamm Business: Kamm & Associates Email: fda.help.now@gmail.com Phone: (847) 3741727

Related Public Records

Same Entity

InBody Co. Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3022764531 InBody Factory #2, Cheonan-si Chungnam, KR
3003193933 BIOSPACE INC. Cerritos, CA, US

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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003074886. Last updated year: 2026. Please use registration number 3003074886 when referencing this establishment in official correspondence.
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