Univec, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Univec, Inc. makes
Univec, Inc. manufactures single-use syringes, including non-reusable locking syringes, auto-disable hypodermic syringes, two-piece syringes, bifurcated sliding sheath syringes, and piston syringes. These products are designed for medical and pharmaceutical applications requiring safe, one-time-use injection delivery.
The company’s portfolio is regulated under FDA Class II medical devices and is listed in the 510(k) premarket notification registry. These devices are based in the United States.
Catalogue
Univec Nonreusable Locking Syringe Ref K951619
510(k) 510(k)Univec Auto-Disable Hypodermic Syringe Ref K993996
510(k) 510(k)Univec Two Piece Syringe Ref K000747
510(k) 510(k)Univec Bifurcated Sliding Sheath Syringe Ref K020500
510(k) 510(k)Univec Non-Reusable Syringe Ref K933469
510(k) 510(k)Piston Syringe Ref K961877
510(k) 510(k)Univec Nonresusable Locking Syringe Ref K943679
510(k) 510(k)
Frequently asked questions
How many devices does Univec, Inc. have in the registry?
The registry currently lists 7 devices for Univec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Univec, Inc.'s devices?
Among its 7 most recently registered devices, Univec, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Univec, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Univec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Univec, Inc. in the registry?
The most recently registered devices listed for Univec, Inc. include UNIVEC NONREUSABLE LOCKING SYRINGE, UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE, UNIVEC TWO PIECE SYRINGE and UNIVEC BIFURCATED SLIDING SHEATH SYRINGE.