Tillotson Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Tillotson Corp. makes
Tillotson Corp. manufactures various types of patient examination gloves, including latex and non-sterile exam gloves.
The company is based in the United States, and its portfolio consists of Class I medical devices that are listed in the FDA 510(k) database.
Catalogue
Latex Examination Gloves Ref K893901
Regimes: 510(k) Registry: 510(k)Non Sterile Exam Gloves ( Tillotson Rubber Co.) Ref K891939
Regimes: 510(k) Registry: 510(k)Hpi Non Sterile Exam Gloves Ref K893018
Regimes: 510(k) Registry: 510(k)Patient Exam Gloves (Mfg. Moss Point Glove Co.) Ref K891940
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tillotson Corp. have in the registry?
The registry currently lists 4 devices for Tillotson Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tillotson Corp.'s devices?
Among its 4 most recently registered devices, Tillotson Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Tillotson Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Tillotson Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tillotson Corp. in the registry?
The most recently registered devices listed for Tillotson Corp. include LATEX EXAMINATION GLOVES, NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.), HPI NON STERILE EXAM GLOVES and PATIENT EXAM GLOVES (MFG. MOSS POINT GLOVE CO.).