Data / Medical devices / United States / Medical Instrument Development Laboratories, Inc.
Medical Instrument Development Laboratories, Inc.: FDA-registered device maker in San Leandro, CA, United States, 4 510(k) clearances
Medical Instrument Development Laboratories, Inc. is registered with the FDA (registration 2935428) in San Leandro, CA, United States. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated April 29, 2016. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2935428
- FEI number
- 1000221463
- Address
- 557 McCormick St, San Leandro, CA, United States, 94577
- Owner or operator
- MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. (2935428)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- August 30, 2005
- Registered through
- 2027
- Brand names listed
- Bi-Blade(TM) Vitreous Cutter, MID LABS, MID Labs, MID Labs Ultimate Vit Enhancer (UVE), MID Labs Vitreous Cutter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Ophthalmic | HMX | 1 | Manufacturer | accessdata.fda.gov |
| Cannula, Trocar, Ophthalmic | NGY | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Vitreous Aspiration And Cutting, Ac-Powered | HQE | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Instrument, Vitreous Aspiration And Cutting, Battery-Powered | HKP | 2 | Manufacturer | accessdata.fda.gov |
| Unit, Phacofragmentation | HQC | 2 | Contract manufacturer | accessdata.fda.gov |
| Vitrectomy, Instrument Cutter | MLZ | 2 | Contract manufacturer | 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 |
|---|---|---|---|---|---|---|
| April 29, 2016 | K153168 | Bi-Blade Vitrectomy Cutter | HQE | Substantially Equivalent | Medical Instrument Development Laboratories | accessdata.fda.gov |
| April 8, 2011 | K102222 | ULTIMATE VIT ENHAMCER (UVE) | HQE | Substantially Equivalent | Medical Instrument Development Laboratories, Inc. | accessdata.fda.gov |
| April 10, 1995 | K950287 | UNIVIT PROBE | HKP | Substantially Equivalent | Medical Instrument Development Laboratories, Inc. | accessdata.fda.gov |
| June 3, 1994 | K932669 | SUPRA-VIT(TM) | HQE | Substantially Equivalent | Medical Instrument Development Laboratories, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Trocar, Ophthalmic
- All makers of Cannula, Ophthalmic
- All makers of Instrument, Vitreous Aspiration And Cutting, Ac-Powered
- All makers of Unit, Phacofragmentation
- All makers of Vitrectomy, Instrument Cutter
- All makers of Instrument, Vitreous Aspiration And Cutting, Battery-Powered
Updated April 29, 2016. 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.