Lenora Glove Pvt , Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Lenora Glove Pvt , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Latex Surgeon’s Gloves Powder Free with protein content labeling claim of 50µg/dm2 or less per glove of extractable protein
1
Total
1
Cleared
0
Denied
Lenora Glove Pvt , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Coimbatore, IN.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Lenora Glove Pvt , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Liberty Management Group , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Lenora Glove Pvt , Ltd.
1 devices