Emg Technology Co., Ltd.
Country not established FDA
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA establishment, FDA recalls
What Emg Technology Co., Ltd. makes
Emg Technology Co., Ltd. manufactures mobility aids, including foldable and standard power wheelchairs (EPW-03, GP-201), middle-wheel drive power chairs (CWD01), and four-wheel scooters (ESG-03). Their product line also covers respiratory and suction devices, such as suction units (SUA01, EMG SUCTION UNIT), compressor nebulizers (EMG NBA02-XXX), handle nebulizers (NB02 SERIES), and a pur oxygen concentrator (CTA01-XXX).
These devices are classified as Class II under FDA regulations and are recorded in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Search and filter all 11 devicesFDA recalls
FDA recall records list 1 recall initiated by Emg Technology Co., Ltd., initiated on 2014-08-03. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2014
- 3 Aug 2014 Z-2642-2014 Class II Terminated suction canister lids may have occluded ports.
FDA establishments
- Emg Technology Co., Ltd. Taichung City · TW FEI 3003803075
Frequently asked questions
How many devices does Emg Technology Co., Ltd. have in the registry?
The registry currently lists 11 devices for Emg Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emg Technology Co., Ltd.'s devices?
Among its 11 most recently registered devices, Emg Technology Co., Ltd. has devices listed in FDA 510(k) (11 devices).
What risk classes do Emg Technology Co., Ltd.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Emg Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Emg Technology Co., Ltd.?
FDA recall records list 1 recall initiated by Emg Technology Co., Ltd., the most recent initiated on 2014-08-03. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Emg Technology Co., Ltd. in the registry?
The most recently registered devices listed for Emg Technology Co., Ltd. include EPW FOLDABLE POWER WHEELCHAIR, EPW-03, MIDDLE WHEEL DRIVE POWER CHAIR, CWD01, EMG MODEL SUA01 SUCTION UNIT and EMG TRITON -COMP, MODEL NCA01-XXX SERIES.
Which FDA establishments are linked to Emg Technology Co., Ltd.?
1 FDA establishment is linked to Emg Technology Co., Ltd. in the registry; they are listed on the company page.