Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medical Instrument Development Laboratories, Inc. — Predicate Candidate Screening
22 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
98 daysmedian FDA review time
306 days90th percentile
22clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K102222 | ULTIMATE VIT ENHAMCER (UVE) | Medical Instrument Development Laboratories, Inc. | 2011-04-08 | 245 | 0 |
| K020911 | MID LABS AUTONOMOUS VIT ENHANCER (AVE) | Medical Instrument Development Laboratories, Inc. | 2002-04-29 | 40 | 0 |
| K992943 | VIT ENHANCER | Medical Instrument Development Laboratories, Inc. | 1999-12-10 | 101 | 0 |
| K971067 | DIGI-INJECTOR | Medical Instrument Development Laboratories, Inc. | 1997-09-19 | 179 | 0 |
| K950287 | UNIVIT PROBE | Medical Instrument Development Laboratories, Inc. | 1995-04-10 | 76 | 0 |
| K934600 | MICRODRIVE | Medical Instrument Development Laboratories, Inc. | 1994-07-27 | 306 | 0 |
| K932669 | SUPRA-VIT(TM) | Medical Instrument Development Laboratories, Inc. | 1994-06-03 | 366 | 0 |
| K932131 | MID LABS TWIN ILLUMINATOR | Medical Instrument Development Laboratories, Inc. | 1994-04-01 | 333 | 0 |
| K924222 | MID LABS, INC. VIT MATE | Medical Instrument Development Laboratories, Inc. | 1993-01-27 | 159 | 0 |
| K851610 | COMBINED MVS SYSTEMS | Medical Instrument Development Laboratories, Inc. | 1985-07-22 | 98 | 0 |
| K851009 | INFUSION SLEEVE - OPHTHALMIC | Medical Instrument Development Laboratories, Inc. | 1985-04-03 | 22 | 0 |
| K850857 | I/A HANDPIECE | Medical Instrument Development Laboratories, Inc. | 1985-03-29 | 28 | 0 |
| K844761 | SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD | Medical Instrument Development Laboratories, Inc. | 1984-12-24 | 17 | 0 |
| K843391 | INFUSION ASPIRATION VITRECTOMY SYS | Medical Instrument Development Laboratories, Inc. | 1984-12-19 | 112 | 0 |
| K842793 | MVS XII | Medical Instrument Development Laboratories, Inc. | 1984-12-19 | 155 | 0 |
| K844131 | NUCLEOTOME | Medical Instrument Development Laboratories, Inc. | 1984-11-29 | 37 | 0 |
| K842471 | AUTOMATED INTRAOCULAR SCISSORS | Medical Instrument Development Laboratories, Inc. | 1984-11-21 | 149 | 0 |
| K834537 | MICRO VIT FRAGMENTATION SYSTEM | Medical Instrument Development Laboratories, Inc. | 1984-03-16 | 98 | 0 |
| K831584 | BAILEY ASPIRATOR/IRRIGATOR | Medical Instrument Development Laboratories, Inc. | 1983-08-12 | 87 | 0 |
| K831192 | INFUSION CANNULA | Medical Instrument Development Laboratories, Inc. | 1983-06-30 | 79 | 0 |
| K831193 | SCLERAL PLUG | Medical Instrument Development Laboratories, Inc. | 1983-06-30 | 79 | 0 |
| K820026 | VITRE CON | Medical Instrument Development Laboratories, Inc. | 1982-02-05 | 31 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda