Devices

Device Recall Tytin Regular Set

Model / Serial
Part Number 29948, Lot Number 3-1294. Expires October 2016
Product Classification
Dental Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Canada, Mexico, Australia, Belgium, Czech Republic, Germany, Spain, France, Great Britain, French Guiana, Italy, Portugal, and Saudi Arabia.
Product Description
Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. || The intended use of this device is to be used as a dental restorative material in the treatment of dental caries.
Manufacturer
Kerr Corporation
1 Event
- Recall of Device Recall Tytin Regular Set

Manufacturer

Kerr Corporation

Manufacturer Address
Kerr Corporation, 28200 Wick Rd, Romulus MI 48174-2639
Manufacturer Parent Company (2017)
Danaher Corporation
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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