Medical Device Manufacturer · US , Mchenry , IL

Jeneric Ind. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1982

Total

Cleared

Denied

Jeneric Ind. has 25 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 25 cleared submissions from 1982 to 1986.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Jeneric Ind. 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 - Jeneric Ind.

25 devices

1-25 of 25

NATURELLE II & LITE II-N72-N74-L

K833774 · EJS

Dental · 89d

Cleared Dec 29, 1983

GOLD-PALLADIUM-SILVER BASED CAST/ALLOY

Jeneric Ind. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Jeneric Ind.

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