Perlink USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Perlink USA, Inc. makes
Perlink USA, Inc. manufactures medical examination gloves, including powder-free and latex options, as well as cassettes and screens for medical use, and clinical thermometers.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Perlink USA, Inc. is based in the US.
Catalogue
Sterling Powder Free Patient Examination Gloves Ref K922358
Regimes: 510(k) Registry: 510(k)Perlink Cassette, Kiran Cassette Ref K896708
Regimes: 510(k) Registry: 510(k)Disposable Latex Examination Gloves Ref K921438
Regimes: 510(k) Registry: 510(k)Sterling Latex Exam Glove, Hypo-Allergenic Ref K924959
Regimes: 510(k) Registry: 510(k)Thermometer, Mercury/Clinical Ref K901790
Regimes: 510(k) Registry: 510(k)Perlink Screen, Kiran Screen Ref K896707
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perlink USA, Inc. have in the registry?
The registry currently lists 6 devices for Perlink USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perlink USA, Inc.'s devices?
Among its 6 most recently registered devices, Perlink USA, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Perlink USA, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Perlink USA, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perlink USA, Inc. in the registry?
The most recently registered devices listed for Perlink USA, Inc. include STERLING POWDER FREE PATIENT EXAMINATION GLOVES, PERLINK CASSETTE, KIRAN CASSETTE, DISPOSABLE LATEX EXAMINATION GLOVES and STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC.