Pentron Laboratory Technologies
Country not established
- Devices
- 5
What Pentron Laboratory Technologies makes
Pentron Laboratory Technologies manufactures dental composite materials and casting alloys, including Sculpture Plus Nano-Hybrid Composite, Sonata Micro Hybrid Composite, Gold Core 35, Gold Core Plus, and Jewel Cast Plus.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Sculpture Plus Nano-Hybrid Composite Ref K023742
Regimes: 510(k) Registry: 510(k)Sonata Micro Hybrid Composite Ref K020555
Regimes: 510(k) Registry: 510(k)Gold Core 35 Ref K023501
Regimes: 510(k) Registry: 510(k)Gold Core Plus Ref K023499
Regimes: 510(k) Registry: 510(k)Jewel Cast Plus Ref K023502
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pentron Laboratory Technologies have in the registry?
The registry currently lists 5 devices for Pentron Laboratory Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pentron Laboratory Technologies's devices?
Among its 5 most recently registered devices, Pentron Laboratory Technologies has devices listed in FDA 510(k) (5 devices).
What risk classes do Pentron Laboratory Technologies's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pentron Laboratory Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pentron Laboratory Technologies in the registry?
The most recently registered devices listed for Pentron Laboratory Technologies include SCULPTURE PLUS NANO-HYBRID COMPOSITE, SONATA MICRO HYBRID COMPOSITE, GOLD CORE 35 and GOLD CORE PLUS.