Genesis Industries, Inc.
Elmwood, WI, US
GENESIS INDUSTRIES, INC. appears in FDA device records in Elmwood, WI. FDA records list 17 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 17 510(k) clearances for Genesis Industries, Inc. between 1983 and 2000. The busiest year on record is 1983, with 11. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 11 |
| 1984 | 2 |
| 1988 | 2 |
| 1997 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K994361 | ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL | MQK | Substantially Equivalent | |
| K962828 | EVERT-IT | HGY | Substantially Equivalent | |
| K880377 | NOVO VIVO MODEL #17140 AND #17135 | GAA | Substantially Equivalent | |
| K880376 | NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP | GBS | Substantially Equivalent | |
| K833290 | C & B 40 PENTRO C & B40 | EIS | Substantially Equivalent | |
| K833287 | SATIN CAST ECONOCAST | EIS | Substantially Equivalent | |
| K833289 | C & B 61 PENTRON C & B61 | EIS | Substantially Equivalent | |
| K833278 | C & B 45 | EIS | Substantially Equivalent | |
| K833280 | SUPRA AP CHOICE 83 | EIS | Substantially Equivalent | |
| K833285 | RX IV PENTRON IV | EIS | Substantially Equivalent | |
| K833288 | C & B57 PENTRON C & B57 | EIS | Substantially Equivalent | |
| K833286 | RX SEG ECONOPLUS | EIS | Substantially Equivalent | |
| K833284 | RX 41 PENTRON 41 | EIS | Substantially Equivalent | |
| K833283 | RX ORY PENTRON C & B | EIS | Substantially Equivalent | |
| K833282 | RX NYSP PENTRON 60 | EIS | Substantially Equivalent | |
| K833281 | RX D PENTRON | EIS | Substantially Equivalent | |
| K833279 | NATURELLE-LITE | EIS | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2183741 | 2183741 | GENESIS INDUSTRIES, INC. | 601 PRO-JECT DR., ELMWOOD, WI 54740 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain