# Medical Instrument Development Laboratories, Inc.

- Location (FDA's records): San Leandro, CA
- FDA decisions: 23 (1982–2016): 23 510(k) clearances
- Names in FDA's records: Medical Instrument Development Laboratories, Inc. (22); Medical Instrument Development Laboratories (1)
- Product codes: HQE (14), HQC (2), HKP (1), EQH (1), LXP (1), HSZ (1), HOY (1), HMX (1), MRH (1)
- Predicates its devices cite: 5 (5 its own); citations of its devices by later devices: 12 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dutch Ophthalmic USA, Inc.: 2 (https://510kreport.com/company/dutch-ophthalmic-usa)
- Clarus Medical, LLC: 1 (https://510kreport.com/company/clarus-medical)
- Dutch Ophthalmic Research Center International BV: 1 (https://510kreport.com/company/dutch-ophthalmic-research-center-international)
- Advanced Medical Optics, Inc.: 1 (https://510kreport.com/company/advanced-medical-optics)
- Bausch and Lomb, Incorporated: 1 (https://510kreport.com/company/bausch-and-lomb)
- Stryker Instruments: 1 (https://510kreport.com/company/stryker-instruments)

## Its most-cited devices
- K932669: Supra-Vit (TM) (1994), cited by 3
- K844131: Nucleotome (1984), cited by 2
- K102222: Ultimate Vit Enhamcer (Uve) (2011), cited by 2
- K020911: Mid Labs Autonomous Vit Enhancer (Ave) (2002), cited by 1
- K924222: Mid Labs, Inc. Vit Mate (1993), cited by 1
- K950287: Univit Probe (1995), cited by 1

## Recent decisions
- K153168: Bi-Blade Vitrectomy Cutter (Apr 29, 2016)
- K102222: Ultimate Vit Enhamcer (Uve) (Apr 8, 2011)
- K020911: Mid Labs Autonomous Vit Enhancer (Ave) (Apr 29, 2002)
- K992943: Vit Enhancer (Dec 10, 1999)
- K971067: Digi-Injector (Sep 19, 1997)
- K950287: Univit Probe (Apr 10, 1995)
- K934600: Microdrive (Jul 27, 1994)
- K932669: Supra-Vit (TM) (Jun 3, 1994)

Source page: https://510kreport.com/company/medical-instrument-development-laboratories