Medical Device Manufacturer · US , Framingham , MA

P.T. Vonix Latexindo Condom (Rubber) Mfg. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2000

Total

Cleared

Denied

P.T. Vonix Latexindo Condom (Rubber) Mfg. has 3 FDA 510(k) cleared medical devices. Based in Framingham, US.

Historical record: 3 cleared submissions from 2000 to 2000. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by P.T. Vonix Latexindo Condom (Rubber) Mfg. Filter by specialty or product code using the sidebar.

P.T. Vonix Latexindo Condom (Rubber) Mfg. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - P.T. Vonix Latexindo Condom (Rubber) Mfg.

3 devices

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