D.T. Davis Enterprises Ltd.
Country not established FDA establishment FEI 3001600982
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 1
Catalogue
Hoverjack Air Patient Lift Device Ref K041503
510(k) 510(k)
Company details
- FDA FEI number
- 3001600982
- Address
- 4482 Innovation Way, Allentown, PA, 18109
FDA recalls
2005
- 13 Sep 2005 Z-0084-06 Unclassified (pre-2012) Terminated Instructions for use are not adhering to the product
Full distribution text
- 13 Sep 2005 Z-0084-06 Unclassified (pre-2012) Terminated Instructions for use are not adhering to the product
Frequently asked questions
How many devices does D.T. DAVIS ENTERPRISES LTD. have in the registry?
The registry currently lists 1 device for D.T. DAVIS ENTERPRISES LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D.T. DAVIS ENTERPRISES LTD.'s devices?
Among its 1 most recently registered device, D.T. DAVIS ENTERPRISES LTD. has devices listed in FDA 510(k) (1 device).
What risk classes do D.T. DAVIS ENTERPRISES LTD.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D.T. DAVIS ENTERPRISES LTD.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for D.T. DAVIS ENTERPRISES LTD.?
FDA recall records list 1 recall initiated by D.T. DAVIS ENTERPRISES LTD., the most recent initiated on 2005-09-13. 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 D.T. DAVIS ENTERPRISES LTD. in the registry?
The most recently registered devices listed for D.T. DAVIS ENTERPRISES LTD. include HOVERJACK AIR PATIENT LIFT DEVICE.