Jeneric Ind.
Jeneric Ind. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1986.
Top product codes for Jeneric Ind.
Recent clearances by Jeneric Ind.
- K862822 — REXILLIUM N. B. F.
- K862926 — SURGICAL VITEX
- K854878 — H40 BASE METAL ALLOY
- K844122 — RX CBG
- K844123 — RX CBY
- K840561 — RX ELAN
- K840563 — RX C & B 20
- K840562 — REX V
- K834560 — VITEX P.D.A
- K833774 — NATURELLE II & LITE II-N72-N74-L
- K833736 — GOLD-PALLADIUM-SILVER BASED CAST/ALLOY
- K833143 — REXILLIUM III
- K833145 — ZENITH
- K833052 — RXG
- K833053 — Y CERAMIC
- K833049 — PALLADENT
- K833050 — RX 90
- K833144 — REX ALLOY
- K823008 — NOVAREX
- K822947 — NEPTUNE
- K822951 — SPHEREX E.C.T.
- K822948 — RX BIOCAST
- K822949 — RX SFC
- K822950 — RX UNIVERSAL
- K820057 — LUXOR PORCELAIN
Data sourced from openFDA. This site is unofficial and independent of the FDA.