Data / Medical devices / United States / Corning Incorporated Discovery Labware
Corning Incorporated Discovery Labware: FDA-registered device maker in Durham, NC, United States, 3 510(k) clearances
Corning Incorporated Discovery Labware is registered with the FDA (registration 1054657) in Durham, NC, United States. It lists 7 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 5, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1054657
- FEI number
- 1000110807
- Address
- 1 Becton Cir, Durham, NC, United States, 27712
- Owner or operator
- Corning Incorporated (1317452)
- Roles
- Complaint file establishment, Contract sterilizer, Manufacturer
- First device listed
- February 15, 2002
- Registered through
- 2026
- Brand names listed
- CellCube Systems and accessories, various styles and sizes, CellSTACK Culture Chambers and accesories, various styles and sizes, Containers, Corning CellBIND roller bottles and accessories;, Corning Closed Systems individually wrapped centrifuge tubes and accessories, Corning Cryogenic vials and accessories;, Corning Easy Grip Storage Bottle and accessories, Corning Erlenmeyer Flasks, various sizes; and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Roller, Tissue Culture | KJC | 1 | Contract sterilizer | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Contract sterilizer | accessdata.fda.gov |
| Dish, Tissue Culture | KIZ | 1 | Complaint file establishment, Contract sterilizer, Manufacturer | accessdata.fda.gov |
| Flask, Tissue Culture | KJA | 1 | Complaint file establishment, Contract sterilizer, Manufacturer | accessdata.fda.gov |
| Labware, Assisted Reproduction | MQK | 2 | Complaint file establishment | accessdata.fda.gov |
| Labware, Assisted Reproduction, Exempt | PUD | 2 | Complaint file establishment | accessdata.fda.gov |
| Spinner, Flask | KJD | 1 | Contract sterilizer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 5, 1999 | K991253 | FALCON IVF ROUND DISH | MQK | Substantially Equivalent | Becton Dickinson Labware | accessdata.fda.gov |
| May 5, 1999 | K991251 | FALCON IVF ONE WELL DISH | MQK | Substantially Equivalent | Becton Dickinson Labware | accessdata.fda.gov |
| May 5, 1999 | K991249 | FALCON IVF FOUR WELL PLATE | MQK | Substantially Equivalent | Becton Dickinson Labware | accessdata.fda.gov |
Compare with other makers
- All makers of Dish, Tissue Culture
- All makers of Container, Specimen, Sterile
- All makers of Labware, Assisted Reproduction, Exempt
- All makers of Flask, Tissue Culture
- All makers of Bottle, Roller, Tissue Culture
Updated May 5, 1999. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.