Taidoc Technology Corporation: FDA filings under this applicant name
FDA lists 123 510(k) clearances under the applicant name “Taidoc Technology Corporation” (first 2004, latest 2024), across 17 product codes in 6 review panels. Median 510(k) review time under this name: 124 days. Since 2017 the median was 241 days, against 195 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 |
|---|---|---|
| 2012 | 8 | 131 |
| 2013 | 5 | 238 |
| 2014 | 0 | — |
| 2015 | 2 | 156 |
| 2016 | 4 | 276 |
| 2017 | 1 | 233 |
| 2018 | 7 | 241 |
| 2019 | 2 | 102 |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 2 | 757 |
| 2023 | 0 | — |
| 2024 | 1 | 925 |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Taidoc Technology Corporation took a median 241 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 195 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| NBW | System, Test, Blood Glucose, Over The Counter | 65 | 65 |
| FLL | Continuous Measurement Thermometer | 16 | 16 |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 11 | 11 |
| CGA | Glucose Oxidase, Glucose | 10 | 10 |
| LFR | Glucose Dehydrogenase, Glucose | 4 | 4 |
| DQA | Oximeter | 3 | 3 |
| CAF | Nebulizer (Direct Patient Interface) | 2 | 2 |
| DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency | 2 | 2 |
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | 2 | 2 |
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 1 | 1 |
Plus 7 more product codes.
Review panels
- Clinical Chemistry (84)
- Cardiovascular (16)
- General Hospital (16)
- Anesthesiology (5)
- Hematology (1)
- General and Plastic Surgery (1)
Most recent Taidoc Technology Corporation 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K221349 | XPER Technology PREMIUM Pro Blood Glucose Monitoring System | PZI | 2024-11-19 | 925 |
| K201037 | FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System | NBW | 2022-06-16 | 787 |
| K200946 | Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) | FLL | 2022-04-05 | 727 |
| K190579 | TD-4183 Blood Glucose Monitoring System | NBW | 2019-06-04 | 90 |
| K182934 | FORA P100 Blood Pressure Monitoring System | DXN | 2019-02-12 | 113 |
| K180863 | FORA NAS100 Electronic Nasal Aspirator, Electronic Nasal Aspirator | BTA | 2018-12-19 | 261 |
| K181675 | FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System | PTC | 2018-12-10 | 168 |
| K181588 | POPS! one Blood Glucose Monitoring System | NBW | 2018-11-30 | 168 |
| K172733 | TD-1035 Thermometer | FLL | 2018-10-22 | 406 |
| K173511 | ActiveCare TD-4121 Blood Glucose Monitoring System | NBW | 2018-07-12 | 241 |
113 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Taidoc Technology Corporation.
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 Taidoc Technology Corporation (a text match, not an official crosswalk):
Frequently asked questions
How many FDA 510(k) clearances are listed under Taidoc Technology Corporation?
FDA lists 123 510(k) clearances under the applicant name “Taidoc Technology Corporation” (first 2004, latest 2024), across 17 product codes in 6 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 Taidoc Technology Corporation?
The median time from FDA receipt to decision across 510(k)s cleared under the name Taidoc Technology Corporation is 124 days. Since 2017: 241 days, versus 195 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Taidoc Technology Corporation?
The most frequent FDA product codes under this applicant name are NBW (System, Test, Blood Glucose, Over The Counter, 65); FLL (Continuous Measurement Thermometer, 16); DXN (System, Measurement, Blood-Pressure, Non-Invasive, 11).
Next steps
- See all 123 Taidoc Technology Corporation clearances with predicates and recalls
- Run predicate analysis for product code NBW, Taidoc Technology Corporation'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, 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.