Temp-Stik Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Temp-Stik Corp. makes
Temp-Stik Corp. manufactures medical devices including a manual skin staple remover for surgical use, a rapid-response thermometer designed for three-second readings, and a reusable adhesive temperature monitoring strip for medical applications.
The company’s products are regulated under FDA Class I and Class II classifications, with some devices subject to 510(k) clearance. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Surgical Products, Skin Staple Remover Ref K822963
Regimes: 510(k) Registry: 510(k)Three Second Thermometer #ts-1000 Ref K820948
Regimes: 510(k) Registry: 510(k)Temp-Stik Model #300 Ref K791558
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Temp-Stik Corp. have in the registry?
The registry currently lists 3 devices for Temp-Stik Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Temp-Stik Corp.'s devices?
Among its 3 most recently registered devices, Temp-Stik Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Temp-Stik Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Temp-Stik Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Temp-Stik Corp. in the registry?
The most recently registered devices listed for Temp-Stik Corp. include SURGICAL PRODUCTS, SKIN STAPLE REMOVER, THREE SECOND THERMOMETER #TS-1000 and TEMP-STIK MODEL #300.