American Pro Latex, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What American Pro Latex, Inc. makes
American Pro Latex, Inc. manufactures single-use latex gloves for medical and examination purposes, including powdered and powder-free variants for surgeons and healthcare professionals. Their portfolio includes exam gloves, surgeon’s gloves, and specialized models like the Gantex NSG-75PF, designed for clinical and procedural use.
All products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Ampro Latex Exam Glove Ref K904740
Regimes: 510(k) Registry: 510(k)Surgeons Glove Powder Free Ref K953358
Regimes: 510(k) Registry: 510(k)Ampro Surgeon's Gloves Ref K910711
Regimes: 510(k) Registry: 510(k)Gantex Model Nsg-75PF Ref K962539
Regimes: 510(k) Registry: 510(k)Powder Free Examination Glove Ref K915157
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Pro Latex, Inc. have in the registry?
The registry currently lists 5 devices for American Pro Latex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Pro Latex, Inc.'s devices?
Among its 5 most recently registered devices, American Pro Latex, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do American Pro Latex, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Pro Latex, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Pro Latex, Inc. in the registry?
The most recently registered devices listed for American Pro Latex, Inc. include AMPRO LATEX EXAM GLOVE, SURGEONS GLOVE POWDER FREE, AMPRO SURGEON'S GLOVES and GANTEX MODEL NSG-75PF.