Medtrol, Inc.
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Medtrol, Inc. makes
Medtrol, Inc. manufactures the Medtrol Dental Kit.
The company is based in the United States, and its product is classified as a Class I medical device listed in the FDA 510(k) registry.
Catalogue
Medtrol Dental Kit Ref K953707
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 1 recall initiated by Medtrol, Inc., initiated on 2009-12-02. By recorded status: 1 terminated. The reasons filed fall into these groups: manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2009
- 2 Dec 2009 Z-1815-2010 Unclassified (pre-2012) Terminated The disinfectant wipes were found out of specifications for the disinfectant activity prior to the expiration date.
Frequently asked questions
How many devices does Medtrol, Inc. have in the registry?
The registry currently lists 1 device for Medtrol, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtrol, Inc.'s devices?
Among its 1 most recently registered device, Medtrol, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtrol, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtrol, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for Medtrol, Inc.?
FDA recall records list 1 recall initiated by Medtrol, Inc., the most recent initiated on 2 Dec 2009. 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 Medtrol, Inc. in the registry?
The most recently registered devices listed for Medtrol, Inc. include MEDTROL DENTAL KIT.