Medical device manufacturer
Taidoc Technology Corporation
Taidoc Technology Corporation holds 123 FDA 510(k) clearances across 17 product codes. Median elapsed review time is 124 days. openFDA lists no recall records naming the company. FDA publishes it under 2 different spellings, all counted here as one company.
Updated · ingest status · JSON
- 510(k) clearances
- 123
- Product codes
- 17
- Median review
- 124 days
- Recall records
- 0
How does FDA spell Taidoc Technology Corporation?
FDA publishes this company under 2 different spellings across its datasets. Every figure on this page counts all of them as one company, which is why the totals here are higher than a search for any single spelling would give you.
| As FDA published it | Dataset | Matched by |
|---|---|---|
| TAIDOC TECHNOLOGY CORPORATION | device/registrationlisting | normalised |
| Taidoc Technology Corporation | device/510k | normalised |
Merges are measured against a hand-labelled sample and held above 98% precision. Pairs the matcher is unsure of are queued for a person rather than merged, because two genuinely different firms with similar names is the error that would corrupt every count on this page.
Which product codes does Taidoc Technology Corporation file in?
17 product codes, ranked by how much they file in each.
| Code | Device | Clearances | Median review | Latest |
|---|---|---|---|---|
| NBW | System, Test, Blood Glucose, Over The Counter | 65 | 119 days | |
| FLL | Continuous Measurement Thermometer | 16 | 72 days | |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 11 | 117 days | |
| CGA | Glucose Oxidase, Glucose | 10 | 94 days | |
| LFR | Glucose Dehydrogenase, Glucose | 4 | 138 days | |
| DQA | Oximeter | 3 | 247 days | |
| CAF | Nebulizer (Direct Patient Interface) | 2 | 238 days | |
| DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency | 2 | 94 days | |
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | 2 | 44 days | |
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 1 | 261 days | |
| DPS | Electrocardiograph | 1 | 270 days | |
| JIN | Nitroprusside, Ketones (Urinary, Non-Quant.) | 1 | 192 days | |
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | 1 | 238 days | |
| LCP | Assay, Glycosylated Hemoglobin | 1 | 498 days | |
| LCX | Kit, Test, Pregnancy, Hcg, Over The Counter | 1 | 312 days | |
| PTC | Uric Acid Test System For At Home Prescription Use | 1 | 168 days | |
| PZI | Prescription Use Blood Glucose Meter For Near-Patient Testing | 1 | 925 days |
Median review is elapsed calendar days between date received and decision date, as published by FDA. It is not FDA review days — the two differ whenever the agency stops the clock for an additional information request.
Source: openFDA device/510k · retrieved
Has Taidoc Technology Corporation had a recall?
openFDA lists no recall records naming this company. That is the absence of a record, not a guarantee — and it counts only recalls FDA has published under a spelling we resolved to this company.
Recall class comes from openFDA's enforcement endpoint, which does not carry every recall — where it is missing, none is shown rather than guessed. Recall class I is the most serious kind of recall; device class I is the least risky kind of device, and the two are never mixed here.
Source: openFDA device/recall · retrieved
What has Taidoc Technology Corporation cleared recently?
| 510(k) | Device | Code | Decision | Elapsed days |
|---|---|---|---|---|
| K221349 | XPER Technology PREMIUM Pro Blood Glucose Monitoring System | PZI | 925 | |
| K201037 | FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System | NBW | 787 | |
| K200946 | Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) | FLL | 727 | |
| K190579 | TD-4183 Blood Glucose Monitoring System | NBW | 90 | |
| K182934 | FORA P100 Blood Pressure Monitoring System | DXN | 113 | |
| K180863 | FORA NAS100 Electronic Nasal Aspirator, Electronic Nasal Aspirator | BTA | 261 | |
| K181675 | FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System | PTC | 168 | |
| K181588 | POPS! one Blood Glucose Monitoring System | NBW | 168 | |
| K172733 | TD-1035 Thermometer | FLL | 406 | |
| K173511 | ActiveCare TD-4121 Blood Glucose Monitoring System | NBW | 241 |
Source: openFDA device/510k · retrieved
Where is Taidoc Technology Corporation registered?
FDA lists 1 registered establishment for this company in US.
Registration means the firm has told FDA it makes or distributes devices from that site. It is not a clearance, an approval or an endorsement.
Watch what Taidoc Technology Corporation files next
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Data on this page comes from FDA's public openFDA API and is US public domain (CC0). DeviceSignal is an independent commercial service and is not affiliated with the U.S. Food and Drug Administration. Information only, not regulatory advice. Verify anything you rely on against open.fda.gov.