H & P Industries, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What H & P Industries, Inc. makes
H & P Industries, Inc. manufactures single-use antiseptic prep pads and towelettes containing providone-iodine, providone-iodine swabsticks, gamma radiation-sterilized alcohol prep pads, lubricating jelly, and ultrasound transmission gel for diagnostic imaging.
The company’s products are regulated under FDA’s Class I, Class II, and Unclassified (U) device categories, with most cleared via the 510(k) pathway. These items are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Providone-Iodine Prep-Pads & Towelettes Ref K830394
510(k) 510(k)Providone-Iodine Swabsticks Ref K830393
510(k) 510(k)Gamma Radiation Sterilized Alcohol Prep Pads Ref K860961
510(k) 510(k)Lubricating Jelly Ref K871169
510(k) 510(k)Tria-Sonic Ultra Sound Transmission Gel Ref K901217
510(k) 510(k)
Frequently asked questions
How many devices does H & P Industries, Inc. have in the registry?
The registry currently lists 5 devices for H & P Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list H & P Industries, Inc.'s devices?
Among its 5 most recently registered devices, H & P Industries, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do H & P Industries, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for H & P Industries, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from H & P Industries, Inc. in the registry?
The most recently registered devices listed for H & P Industries, Inc. include PROVIDONE-IODINE PREP-PADS & TOWELETTES, PROVIDONE-IODINE SWABSTICKS, GAMMA RADIATION STERILIZED ALCOHOL PREP PADS and LUBRICATING JELLY.