Healthcare Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Healthcare Technologies, Inc. makes
Healthcare Technologies, Inc. manufactures single-lumen and dual-lumen central venous catheters, including the UNIPORT models SD-60, SD-70, SD-90, TD-60, TD-70, and TD-90. These catheters are designed for intravenous access in medical settings, supporting fluid administration, blood draws, and monitoring.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The devices are intended for use in the United States.
Catalogue
Uniport Model Sd-60, Sd-70 Ref K870950
Regimes: 510(k) Registry: 510(k)HCT Empty EVA Container Pack Ref K190328
Regimes: 510(k) Registry: 510(k)Uniport Models Sd-90, Td-60, Td-70 & Td-90 Ref K873575
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Healthcare Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Healthcare Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Healthcare Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Healthcare Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Healthcare Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Healthcare Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Healthcare Technologies, Inc. in the registry?
The most recently registered devices listed for Healthcare Technologies, Inc. include UNIPORT MODEL SD-60, SD-70, HCT Empty EVA Container Pack and UNIPORT MODELS SD-90, TD-60, TD-70 & TD-90.