Shenzhen Comen Medical Instruments Co.,Ltd: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Shenzhen Comen Medical Instruments Co.,Ltd” (first 2018, latest 2025), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 283 days. Since 2017 the median was 283 days, against 160 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
20181283
20191232
20200—
20210—
20221582
20230—
20240—
20252295
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Shenzhen Comen Medical Instruments Co.,Ltd took a median 283 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 160 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)44
JOWSleeve, Limb, Compressible11

Review panels

Most recent Shenzhen Comen Medical Instruments Co.,Ltd 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K250854Multi-parameter Patient Monitor (N10); Multi-parameter Patient Monitor (N12); Multi-parameter Patient Monitor (N15); Multi-parameter Patient Monitor (N10MPro); Multi-parameter Patient Monitor (N12MPro); Multi-parameter Patient Monitor (N15MPro)MHX2025-12-17271
K250190Sequential Compression System (SCD600)JOW2025-12-08319
K211619Multi-Parameter Patient MonitorMHX2022-12-29582
K191106C50 and C80 Multi-parameter Patient MonitorMHX2019-12-13232
K173454Multi-parameter Patient Monitor, models C30MHX2018-08-16283

Recalls

openFDA lists no recalls under a recalling firm named Shenzhen Comen Medical Instruments 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.

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 Shenzhen Comen Medical Instruments Co.,Ltd?

FDA lists 5 510(k) clearances under the applicant name “Shenzhen Comen Medical Instruments Co.,Ltd” (first 2018, latest 2025), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Shenzhen Comen Medical Instruments Co.,Ltd?

The median time from FDA receipt to decision across 510(k)s cleared under the name Shenzhen Comen Medical Instruments Co.,Ltd is 283 days. Since 2017: 283 days, versus 160 days for all cleared 510(k)s in the same product codes.

Which FDA product codes appear under Shenzhen Comen Medical Instruments Co.,Ltd?

The most frequent FDA product codes under this applicant name are MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms), 4); JOW (Sleeve, Limb, Compressible, 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, with punctuation and legal suffixes removed; 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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