Perry, Div.
Country not established
- Devices
- 6
What Perry, Div. makes
Perry, Div. manufactures single-use surgical gloves designed for patient and operator protection during procedures, along with suturing sets that include anesthetic for localized pain management. Their portfolio also includes Kelly cholangiocaths for biliary drainage, basic suturing sets, disposable lancing blades and scalpel handles, and intravenous starter kits for vein access.
These products are regulated under FDA Class I and Class II classifications, with most cleared via the 510(k) pathway. The company’s devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Perry Dermaguard Surgical Gloves Ref K843125
Regimes: 510(k) Registry: 510(k)Perry Suturing Set W/Anesthetic Ref K844610
Regimes: 510(k) Registry: 510(k)Kelly Cholangiocath Ref K833920
Regimes: 510(k) Registry: 510(k)Perry Suturing Set Ref K844609
Regimes: 510(k) Registry: 510(k)Lance Blades & Scalpels Ref K844001
Regimes: 510(k) Registry: 510(k)I.V. Start Kit Ref K851226
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perry, Div. have in the registry?
The registry currently lists 6 devices for Perry, Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perry, Div.'s devices?
Among its 6 most recently registered devices, Perry, Div. has devices listed in FDA 510(k) (6 devices).
What risk classes do Perry, Div.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Perry, Div.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perry, Div. in the registry?
The most recently registered devices listed for Perry, Div. include PERRY DERMAGUARD SURGICAL GLOVES, PERRY SUTURING SET W/ANESTHETIC, KELLY CHOLANGIOCATH and PERRY SUTURING SET.