Albors-Menconi Latex Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Albors-Menconi Latex Corp. makes
Albors-Menconi Latex Corp. manufactures single-use patient examination gloves and sterile surgeons' gloves, both made from latex. These products are designed for clinical and procedural use to maintain sterility and reduce cross-contamination during medical examinations and surgical procedures.
The company’s portfolio is regulated under FDA’s Class I device classification, requiring compliance with 510(k) clearance for market authorisation. The devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891620
Regimes: 510(k) Registry: 510(k)Sterile Surgeons' Gloves Ref K891621
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Albors-Menconi Latex Corp. have in the registry?
The registry currently lists 2 devices for Albors-Menconi Latex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Albors-Menconi Latex Corp.'s devices?
Among its 2 most recently registered devices, Albors-Menconi Latex Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Albors-Menconi Latex Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Albors-Menconi Latex Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Albors-Menconi Latex Corp. in the registry?
The most recently registered devices listed for Albors-Menconi Latex Corp. include PATIENT EXAMINATION GLOVES (LATEX) and STERILE SURGEONS' GLOVES.