Medlogic Global Corp.
Country not established
- Devices
- 8
What Medlogic Global Corp. makes
Medlogic Global Corp. manufactures topical skin adhesives, including the Liquiband Dental and Superskin product lines.
The company is based in the United States, and its portfolio consists of Class I and Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Liquiband Dental Ref K993556
Regimes: 510(k) Registry: 510(k)Liquishield Liquid Bandage, Model Lsb 0001 Ref K031321
Regimes: 510(k) Registry: 510(k)Liquiband Ultima, Lut 003 Ref K100284
Regimes: 510(k) Registry: 510(k)Liquiband Ultima, Model LB0004 Ref K083531
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Liquiband Flow Control Ref K110184
Regimes: 510(k) Registry: 510(k)Liquiband Dual, Model Lbd 001 Ref K102076
Regimes: 510(k) Registry: 510(k)Superskin Ref K972081
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medlogic Global Corp. have in the registry?
The registry currently lists 8 devices for Medlogic Global Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medlogic Global Corp.'s devices?
Among its 8 most recently registered devices, Medlogic Global Corp. has devices listed in FDA 510(k) (8 devices).
What risk classes do Medlogic Global Corp.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Medlogic Global Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medlogic Global Corp. in the registry?
The most recently registered devices listed for Medlogic Global Corp. include LIQUIBAND DENTAL, LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001, LIQUIBAND ULTIMA, LUT 003 and LIQUIBAND ULTIMA, MODEL LB0004.