Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Modern Medical Equipment Mfg., Ltd. · Predicate Candidate Screening
14 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
233 daysmedian FDA review time
459 days90th percentile
14clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K093479 | DISPOSABLE SUCTION AND IRRIGATION SYSTEM | Modern Medical Equipment Mfg., Ltd. | 2010-05-19 | 191 | 0 |
| K091511 | MODERN MEDICAL RESECTOSCOPE ELECTRODES | Modern Medical Equipment Mfg., Ltd. | 2010-01-15 | 238 | 0 |
| K070812 | DISPOSABLE LAPAROSCOPIC INSTRUMENT | Modern Medical Equipment Mfg., Ltd. | 2007-09-14 | 172 | 0 |
| K070877 | ENDOCERVICAL ELECTRODE # 2 | Modern Medical Equipment Mfg., Ltd. | 2007-07-27 | 120 | 0 |
| K050842 | AGCEL WOUND DRESSING,AGCEL BURN DRESSING | Modern Medical Equipment Mfg., Ltd. | 2006-08-02 | 488 | 0 |
| K043036 | NON-STICK ELECTRODE | Modern Medical Equipment Mfg., Ltd. | 2005-05-06 | 183 | 0 |
| K033095 | SMOKE EVACUATION ATTACHEMENT | Modern Medical Equipment Mfg., Ltd. | 2004-11-17 | 415 | 0 |
| K040238 | SOFTSEAL HSG CATHETER | Modern Medical Equipment Mfg., Ltd. | 2004-06-22 | 148 | 0 |
| K030831 | LAPASCOPIC INSTRUMENTS AND ELECTRODE TIPS | Modern Medical Equipment Mfg., Ltd. | 2004-06-15 | 459 | 0 |
| K032327 | MODERN MEDICAL BIPOLAR FORCEPS | Modern Medical Equipment Mfg., Ltd. | 2004-06-15 | 323 | 0 |
| K032965 | LAPAROSCOPIC INSTRUMENT, ELECTRODE AND CABLE | Modern Medical Equipment Mfg., Ltd. | 2004-05-13 | 233 | 0 |
| K033003 | SUCTION COAGULATOR | Modern Medical Equipment Mfg., Ltd. | 2004-05-13 | 231 | 1 |
| K023506 | SURGICAL MEDICAL DEVICE CAUTERY | Modern Medical Equipment Mfg., Ltd. | 2004-01-13 | 452 | 0 |
| K023966 | DISPOSABLE BI-POLAR CABLE | Modern Medical Equipment Mfg., Ltd. | 2003-02-27 | 90 | 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