Health & Life Co., Ltd.: FDA filings under this applicant name

FDA lists 60 510(k) clearances under the applicant name “Health & Life Co., Ltd.” (first 1999, latest 2021), across 6 product codes in 5 review panels. Median 510(k) review time under this name: 50 days. Since 2017 the median was 145 days, against 190 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
20123135
20133106
2014166
20151190
2016651
20170—
20181261
20193136
20201102
20212158
20220—
20230—
20240—
20250—
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Health & Life Co., Ltd. took a median 145 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 190 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
DXNSystem, Measurement, Blood-Pressure, Non-Invasive5555
CAFNebulizer (Direct Patient Interface)11
DQDStethoscope, Electronic11
FLLContinuous Measurement Thermometer11
MNWAnalyzer, Body Composition11
NBWSystem, Test, Blood Glucose, Over The Counter11

Review panels

Most recent Health & Life Co., Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K211744Non-Contact Infrared Thermometer, model HL710HFLL2021-11-24170
K211127Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DMDXN2021-09-08145
K200521Full Automatic(NIBP) Blood Pressure MonitorDXN2020-06-12102
K190507Full Automatic (NIBP) Blood Pressure MonitorDXN2019-09-16199
K190133Full Automatic (NIBP) Blood Pressure Monitor-HL158UBDXN2019-06-13136
K190134Full Automatic (NIBP) Blood Pressure Monitor-HL158TBDXN2019-05-20112
K180240Full Automatic(NIBP) Blood Pressure MonitorDXN2018-10-17261
K162338Full Automatic (NIBP) Blood Pressure MonitorDXN2016-09-2130
K160557Full Automatic (NIBP) Blood Pressure MonitorDXN2016-07-06128
K161156Full Automatic (NIBP) Blood Pressure MonitorDXN2016-06-1450

50 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Health & Life Co., Ltd..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Related HCPCS codes

HCPCS Level II codes whose descriptors match the device names of the product codes filed under Health & Life Co., Ltd. (a text match, not an official crosswalk):

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Health & Life Co., Ltd.?

FDA lists 60 510(k) clearances under the applicant name “Health & Life Co., Ltd.” (first 1999, latest 2021), across 6 product codes in 5 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Health & Life Co., Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Health & Life Co., Ltd. is 50 days. Since 2017: 145 days, versus 190 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Health & Life Co., Ltd.?

The most frequent FDA product codes under this applicant name are DXN (System, Measurement, Blood-Pressure, Non-Invasive, 55); CAF (Nebulizer (Direct Patient Interface), 1); DQD (Stethoscope, Electronic, 1).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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