Health Development Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Health Development Corp. makes
Health Development Corp. manufactures enteric feeding products, including the KEOFEED Easy-Fill Enteric Feed Bag for nutrient delivery, the PEM-C and SURGIFEED for postoperative or long-term gastrointestinal feeding, and percutaneous gastrointestinal tubes for direct feeding access. The company also produces a seminal collection device for assisted reproduction procedures.
The portfolio includes Class I and Class II devices, with submissions recorded in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Keofeed (R) Easy-Fill Enteric Feed Bag Ref K802482
Regimes: 510(k) Registry: 510(k)Pem-C Ref K830397
Regimes: 510(k) Registry: 510(k)Surgifeed Ref K791714
Regimes: 510(k) Registry: 510(k)Percutaneous Gastrointestinal Tube Ref K810499
Regimes: 510(k) Registry: 510(k)Seminal Collection Device Ref K823937
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Health Development Corp. have in the registry?
The registry currently lists 5 devices for Health Development Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Health Development Corp.'s devices?
Among its 5 most recently registered devices, Health Development Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Health Development Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Health Development Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Health Development Corp. in the registry?
The most recently registered devices listed for Health Development Corp. include KEOFEED (R) EASY-FILL ENTERIC FEED BAG, PEM-C, SURGIFEED and PERCUTANEOUS GASTROINTESTINAL TUBE.