Devices

Device Recall PowerProMax

Model / Serial
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution including United States.
Product Description
PowerProMax PRO5100M Battery Single Trigger, || PowerProMax PRO5200M Battery Two Trigger, || PowerProMax PRO5250M Battery Two-Trigger Standard, || PowerProMax PRO5300M Battery Oscillator, || PowerProMax PRO5400M Battery Reciprocator, and || PowerProMax PRO6200 Battery Single Trigger. || CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA.
Manufacturer
Linvatec Corp. dba ConMed Linvatec
1 Event
- Recall of Device Recall PowerProMax

Manufacturer

Linvatec Corp. dba ConMed Linvatec

Manufacturer Address
Linvatec Corp. dba ConMed Linvatec, 11311 Concept Blvd, Largo FL 33773-4908
Manufacturer Parent Company (2017)
CONMED Corp.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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