Needle Tech Products, Inc.
United StatesFDA applicant, unverified FDA FEI 3006283319
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Needle Tech Products, Inc. makes
Needle Tech Products, Inc. manufactures guidewire introducer needles, marrow aspiration needle kits, and Galt Tork devices.
The company is based in the United States, and its portfolio includes Class I and Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3006283319
- Address
- 452 John L Dietsch Blvd, N Attleboro, MA, 02763
Frequently asked questions
How many devices does Needle Tech Products, Inc. have in the registry?
The registry currently lists 3 devices for Needle Tech Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Needle Tech Products, Inc.'s devices?
Among its 3 most recently registered devices, Needle Tech Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Needle Tech Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Needle Tech Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Needle Tech Products, Inc. in the registry?
The most recently registered devices listed for Needle Tech Products, Inc. include NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013, MARROMAX B ONE MARROW ASPIRATION NEEDLE KIT, MODELS 50083-XX, 50084-XX and Galt Tork, 0.010 to 0.020 inches (yellow), Galt Tork, 0.025 to 0.040 inches (orange).