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Genesis Industries, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2183741

Devices
17
Registrations
FDA
FDA recalls
0

Catalogue17

Newest first, rows 1-17 of 17

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  • C & B 45 Ref K833278

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rx D Pentron Ref K833281

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rx Ory Pentron C & B Ref K833283

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rx Iv Pentron Iv Ref K833285

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Novo Vivo Suction Catheter Vessel W/Mucose Trap Ref K880376

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rx Nysp Pentron 60 Ref K833282

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Esp Four Well Tissue Culture Plate, Esp Six Well Tissue Culture Plate, Esp Micro Six Well Tissue Culture Plate, Esp Well Ref K994361

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Supra Ap Choice 83 Ref K833280

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • C & B 61 Pentron C & B61 Ref K833289

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Novo Vivo Model #17140 And #17135 Ref K880377

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rx 41 Pentron 41 Ref K833284

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Naturelle-Lite Ref K833279

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Evert-It Ref K962828

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rx Seg Econoplus Ref K833286

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • C & B57 Pentron C & B57 Ref K833288

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • C & B 40 Pentro C & B40 Ref K833290

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Satin Cast Econocast Ref K833287

    Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 1-17 of 17

Company details

FDA FEI number
2183741
Address
601 PRO-JECT DR., ELMWOOD, WI, 54740

Frequently asked questions

How many devices does GENESIS INDUSTRIES, INC. have in the registry?

The registry currently lists 17 devices for GENESIS INDUSTRIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list GENESIS INDUSTRIES, INC.'s devices?

Among its 17 most recently registered devices, GENESIS INDUSTRIES, INC. has devices listed in FDA 510(k) (17 devices).

What risk classes do GENESIS INDUSTRIES, INC.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for GENESIS INDUSTRIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from GENESIS INDUSTRIES, INC. in the registry?

The most recently registered devices listed for GENESIS INDUSTRIES, INC. include C & B 45, RX D PENTRON, RX ORY PENTRON C & B and RX IV PENTRON IV.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.