Microlife Intellectual Property GmbH: FDA filings under this applicant name

FDA lists 54 510(k) clearances under the applicant name “Microlife Intellectual Property GmbH” (first 2003, latest 2023), across 3 product codes in 3 review panels. Median 510(k) review time under this name: 78 days. Since 2017 the median was 195 days, against 183 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
20122133
2013128
20141116
2015326
20161112
20173176
20182235
20193100
20203133
20212196
20221265
20233198
20240—
20250—
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Microlife Intellectual Property GmbH took a median 195 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 183 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
DXNSystem, Measurement, Blood-Pressure, Non-Invasive3333
FLLContinuous Measurement Thermometer2020
BZHMeter, Peak Flow, Spirometry11

Review panels

Most recent Microlife Intellectual Property GmbH 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K230075Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5KDXN2023-06-28169
K222979Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5WDXN2023-05-19233
K222153Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR)DXN2023-02-03198
K211776Microlife Non-Contact Infrared Forehead Thermometer, Model FR1MF1-B (NC150 BT)FLL2022-03-01265
K211288Microlife Wrist Watch Blood Pressure Monitor Model BP3GK1-4BDXN2021-11-04190
K202729Microlife Upper Arm Automatic Digital Blood Pressure MonitorDXN2021-04-08202
K200738Microlife Upper Arm Automatic Digital Blood Pressure MonitorDXN2020-07-23122
K200297Microlife Upper Arm Automatic Digital Blood Pressure MonitorDXN2020-06-18133
K191829Microlife Non-Contact Infrared Forehead ThermometerFLL2020-02-13219
K183663Microlife Digital Infrared Ear ThermometerFLL2019-07-16201

44 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Microlife Intellectual Property GmbH.

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.

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 Microlife Intellectual Property GmbH?

FDA lists 54 510(k) clearances under the applicant name “Microlife Intellectual Property GmbH” (first 2003, latest 2023), across 3 product codes in 3 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 Microlife Intellectual Property GmbH?

The median time from FDA receipt to decision across 510(k)s cleared under the name Microlife Intellectual Property GmbH is 78 days. Since 2017: 195 days, versus 183 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Microlife Intellectual Property GmbH?

The most frequent FDA product codes under this applicant name are DXN (System, Measurement, Blood-Pressure, Non-Invasive, 33); FLL (Continuous Measurement Thermometer, 20); BZH (Meter, Peak Flow, Spirometry, 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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