Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
The Tulip Mfg. Co. · Predicate Candidate Screening
24 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
126 daysmedian FDA review time
144 days90th percentile
24clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K952906 | THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK | The Tulip Mfg. Co. | 1996-01-22 | 213 | 0 |
| K952959 | THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK | The Tulip Mfg. Co. | 1996-01-22 | 210 | 0 |
| K955502 | THE TULIP MONO POLAR ROTATABLE METZ SCISSORS | The Tulip Mfg. Co. | 1996-01-17 | 47 | 0 |
| K955501 | THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP | The Tulip Mfg. Co. | 1996-01-17 | 47 | 0 |
| K952902 | THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR | The Tulip Mfg. Co. | 1995-11-14 | 144 | 0 |
| K952951 | THE TULIP COMPANY BRASON NERVE HOOK & DISSECTOR | The Tulip Mfg. Co. | 1995-11-14 | 141 | 0 |
| K952932 | THE TULIP COMPANY BRANSON #1 ELEVATOR | The Tulip Mfg. Co. | 1995-11-14 | 141 | 0 |
| K952953 | THE TULIP CXOMPANY BRANSON #2 ELEVATOR | The Tulip Mfg. Co. | 1995-11-14 | 141 | 0 |
| K952901 | THE TULIP COMPANY BRANSON #1 & #2 ELEVATOR | The Tulip Mfg. Co. | 1995-11-14 | 144 | 0 |
| K954734 | THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATIO | The Tulip Mfg. Co. | 1995-11-14 | 42 | 0 |
| K952958 | THE TULIP COMPANY BRANSON OVERSHEATH | The Tulip Mfg. Co. | 1995-11-14 | 141 | 0 |
| K952955 | THE TULIP COMPANY BRANSON STRAIGHT DISSECTOR | The Tulip Mfg. Co. | 1995-10-30 | 126 | 0 |
| K952899 | THE TULIP INSULATED SCISSORS | The Tulip Mfg. Co. | 1995-10-30 | 129 | 0 |
| K952936 | THE TULIP COMPANY BRANSON ANTERIOR ELEVATOR | The Tulip Mfg. Co. | 1995-10-30 | 126 | 0 |
| K952900 | THE TULIP COMPANY BRANSON SOFT TISSUE RETRACTOR | The Tulip Mfg. Co. | 1995-10-30 | 129 | 0 |
| K952934 | THE TULIP COMPANY BRANSON RECURVED DISSECTOR | The Tulip Mfg. Co. | 1995-10-30 | 126 | 0 |
| K952957 | THE TULIP INSULATED GRASPERS | The Tulip Mfg. Co. | 1995-10-30 | 126 | 0 |
| K952954 | THE TULIP COMPANY WEIL-BLAKESLEY FORCEPS | The Tulip Mfg. Co. | 1995-10-30 | 126 | 0 |
| K952956 | THE TULIP COMPANY BRANSON DOUBLE-ENDED DISSECTOR | The Tulip Mfg. Co. | 1995-10-30 | 126 | 0 |
| K952980 | THE TULIP LARGE SOFT TISSUE RETRACTOR | The Tulip Mfg. Co. | 1995-09-29 | 95 | 0 |
| K952935 | THE TULIP SMALL SOFT TISSUE RETRACTOR | The Tulip Mfg. Co. | 1995-09-29 | 95 | 0 |
| K952965 | THE TULIP J DISSECTOR | The Tulip Mfg. Co. | 1995-09-22 | 87 | 0 |
| K952973 | THE TULIP MONO-POLAR CAUTERY SPATULA | The Tulip Mfg. Co. | 1995-09-11 | 76 | 0 |
| K952563 | THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM | The Tulip Mfg. Co. | 1995-07-25 | 53 | 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