Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account
Micro Surgical Instruments Corp. — Predicate Candidate Screening
15 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
208 days90th percentile
15clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K931395 | SERIES 5000 BATTERY POWERED INSTRUMENT SYSTEM | Micro Surgical Instruments Corp. | 1994-01-28 | 315 | 0 |
| K932492 | IMPLANTOLOGY MODULE, MODEL 2175 | Micro Surgical Instruments Corp. | 1993-10-05 | 134 | 0 |
| K930205 | ELECTRIC WIRE DRIVER, MODEL 2640E | Micro Surgical Instruments Corp. | 1993-08-02 | 199 | 0 |
| K914998 | MICROAIRE(R) FACIAL BONE PLATING SYSTEM | Micro Surgical Instruments Corp. | 1992-06-02 | 208 | 0 |
| K915139 | MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE | Micro Surgical Instruments Corp. | 1992-02-05 | 84 | 0 |
| K914346 | DRILL MODULES MODELS 2116/2117 | Micro Surgical Instruments Corp. | 1991-11-27 | 61 | 0 |
| K913369 | MICRO-AIRE MODEL 2060 | Micro Surgical Instruments Corp. | 1991-11-01 | 95 | 0 |
| K913266 | MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS | Micro Surgical Instruments Corp. | 1991-10-21 | 90 | 0 |
| K910175 | FIXATION DEVICES AND BONE PLATE | Micro Surgical Instruments Corp. | 1991-06-21 | 157 | 0 |
| K905383 | 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY | Micro Surgical Instruments Corp. | 1991-06-18 | 201 | 0 |
| K905207 | MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESS | Micro Surgical Instruments Corp. | 1991-01-22 | 63 | 0 |
| K905277 | MICRO-AIRE 4220-000 OSCILLATING SAW | Micro Surgical Instruments Corp. | 1991-01-08 | 46 | 0 |
| K905097 | MICRO-AIRE MODEL NUMBER: MK-426 | Micro Surgical Instruments Corp. | 1990-12-21 | 38 | 0 |
| K905187 | BONE RASPS | Micro Surgical Instruments Corp. | 1990-12-19 | 30 | 0 |
| K894301 | MICRO-AIRE STERNUM SAW 4800 | Micro Surgical Instruments Corp. | 1989-08-03 | 41 | 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