Genesis Industries, Inc.
Genesis Industries, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2000.
Top product codes for Genesis Industries, Inc.
Recent clearances by Genesis Industries, Inc.
- K994361 — ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL
- K962828 — EVERT-IT
- K880377 — NOVO VIVO MODEL #17140 AND #17135
- K880376 — NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP
- K833287 — SATIN CAST ECONOCAST
- K833290 — C & B 40 PENTRO C & B40
- K833278 — C & B 45
- K833289 — C & B 61 PENTRON C & B61
- K833280 — SUPRA AP CHOICE 83
- K833285 — RX IV PENTRON IV
- K833288 — C & B57 PENTRON C & B57
- K833279 — NATURELLE-LITE
- K833281 — RX D PENTRON
- K833282 — RX NYSP PENTRON 60
- K833283 — RX ORY PENTRON C & B
- K833284 — RX 41 PENTRON 41
- K833286 — RX SEG ECONOPLUS
Data sourced from openFDA. This site is unofficial and independent of the FDA.