Medical Instrument Development Laboratories, Inc.
San Leandro, CA, US
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. appears in FDA device records in San Leandro, CA. FDA records list 23 510(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 23 510(k) clearances for Medical Instrument Development Laboratories, Inc. between 1982 and 2016. The busiest year on record is 1984, with 6. The most recent is 2016, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1983 | 3 |
| 1984 | 6 |
| 1985 | 3 |
| 1993 | 1 |
| 1994 | 3 |
| 1995 | 1 |
| 1997 | 1 |
| 1999 | 1 |
| 2002 | 1 |
| 2011 | 1 |
| 2016 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K153168 | Bi-Blade Vitrectomy Cutter | HQE | Substantially Equivalent | |
| K102222 | ULTIMATE VIT ENHAMCER (UVE) | HQE | Substantially Equivalent | |
| K020911 | MID LABS AUTONOMOUS VIT ENHANCER (AVE) | HQE | Substantially Equivalent | |
| K992943 | VIT ENHANCER | HQE | Substantially Equivalent | |
| K971067 | DIGI-INJECTOR | MRH | Substantially Equivalent | |
| K950287 | UNIVIT PROBE | HKP | Substantially Equivalent | |
| K934600 | MICRODRIVE | HQE | Substantially Equivalent | |
| K932669 | SUPRA-VIT(TM) | HQE | Substantially Equivalent | |
| K932131 | MID LABS TWIN ILLUMINATOR | EQH | Substantially Equivalent | |
| K924222 | MID LABS, INC. VIT MATE | HQE | Substantially Equivalent | |
| K851610 | COMBINED MVS SYSTEMS | HQE | Substantially Equivalent | |
| K851009 | INFUSION SLEEVE - OPHTHALMIC | HQC | Substantially Equivalent | |
| K850857 | I/A HANDPIECE | HQE | Substantially Equivalent | |
| K844761 | SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD | HOY | Substantially Equivalent | |
| K843391 | INFUSION ASPIRATION VITRECTOMY SYS | HQE | Substantially Equivalent | |
| K842793 | MVS XII | HQE | Substantially Equivalent | |
| K844131 | NUCLEOTOME | HSZ | Substantially Equivalent | |
| K842471 | AUTOMATED INTRAOCULAR SCISSORS | HQE | Substantially Equivalent | |
| K834537 | MICRO VIT FRAGMENTATION SYSTEM | HQC | Substantially Equivalent | |
| K831584 | BAILEY ASPIRATOR/IRRIGATOR | HQE | Substantially Equivalent | |
| K831193 | SCLERAL PLUG | LXP | Substantially Equivalent | |
| K831192 | INFUSION CANNULA | HMX | Substantially Equivalent | |
| K820026 | VITRE CON | HQE | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2935428 | 1000221463 | MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. | 557 McCormick St, SAN LEANDRO, CA 94577 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- HMXCannula, Ophthalmic
- NGYCannula, Trocar, Ophthalmic
- HSZInstrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment
- HQEInstrument, Vitreous Aspiration And Cutting, Ac-Powered
- HKPInstrument, Vitreous Aspiration And Cutting, Battery-Powered
- LXPPlug, Scleral
- MRHPump, Infusion, Ophthalmic
- HOYShield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- EQHSource, Carrier, Fiberoptic Light
- HQCUnit, Phacofragmentation
- MLZVitrectomy, Instrument Cutter
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