Shenzhen Caremed Medical Technology Co., Ltd.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Shenzhen Caremed Medical Technology Co., Ltd.” (first 2016, latest 2019), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 275 days. Since 2017 the median was 207 days, against 194 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
| Year | Clearances | Median review days |
|---|---|---|
| 2016 | 1 | 356 |
| 2017 | 1 | 428 |
| 2018 | 2 | 93 |
| 2019 | 2 | 275 |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Shenzhen Caremed Medical Technology Co., Ltd. took a median 207 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 194 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| DQA | Oximeter | 2 | 2 |
| FLL | Continuous Measurement Thermometer | 2 | 2 |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) | 1 | 1 |
| DXQ | Blood Pressure Cuff | 1 | 1 |
Review panels
- Anesthesiology (2)
- Cardiovascular (2)
- General Hospital (2)
Most recent Shenzhen Caremed Medical Technology Co., Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K191279 | Disposable SpO2 Sensor | DQA | 2019-12-06 | 207 |
| K182751 | Reusable Temperature Probe | FLL | 2019-09-06 | 343 |
| K182755 | Disposable Temperature Probe | FLL | 2018-12-21 | 84 |
| K182433 | Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff | DXQ | 2018-12-17 | 102 |
| K153184 | Caremed Reusable & Disposable SPO2 Sensors | DQA | 2017-01-04 | 428 |
| K153188 | Caremed patient cable and leadwires | DSA | 2016-10-24 | 356 |
Recalls
openFDA lists no recalls under a recalling firm named Shenzhen Caremed Medical Technology 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.
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (159 510(k)s)
- Shenzhen Dongdixin Technology Co., Ltd. (26 510(k)s)
- Shenzhen Kaiyan Medical Equipment Co., Ltd. (24 510(k)s)
- Shenzhen TPH Technology Co., Ltd. (24 510(k)s)
- Shenzhen Ulike Smart Electronics Co., Ltd. (23 510(k)s)
- Shenzhen AOJ Medical Technology Co., Ltd. (17 510(k)s)
- Shenzhen Beacon Display Technology Co., Ltd. (17 510(k)s)
- Shenzhen Med-Link Electronics Tech Co., Ltd. (14 510(k)s)
- Shenzhen Root Innovation Technology Co., Ltd. (13 510(k)s)
- Shenzhen Osto Technology Company Limited (12 510(k)s)
- Shenzhen RF Tech Co., Ltd. (12 510(k)s)
- Shenzhen Creative Industry Co., Ltd. (11 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Shenzhen Caremed Medical Technology Co., Ltd.?
FDA lists 6 510(k) clearances under the applicant name “Shenzhen Caremed Medical Technology Co., Ltd.” (first 2016, latest 2019), across 4 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 Shenzhen Caremed Medical Technology Co., Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Shenzhen Caremed Medical Technology Co., Ltd. is 275 days. Since 2017: 207 days, versus 194 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Shenzhen Caremed Medical Technology Co., Ltd.?
The most frequent FDA product codes under this applicant name are DQA (Oximeter, 2); FLL (Continuous Measurement Thermometer, 2); DSA (Cable, Transducer And Electrode, Patient, (Including Connector), 1).
Next steps
- See all 6 Shenzhen Caremed Medical Technology Co., Ltd. clearances with predicates and recalls
- Run predicate analysis for product code DQA, Shenzhen Caremed Medical Technology Co., Ltd.'s most frequent
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.