Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Peregrine Surgical , Ltd. — Predicate Candidate Screening
19 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
88 daysmedian FDA review time
221 days90th percentile
19clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K151604 | 23ga Chandelier Illuminator, 25ga Chandelier Illuminator | Peregrine Surgical , Ltd. | 2015-09-11 | 88 | 0 |
| K132614 | PEREGRINE CURVED ILLUMINATING LASER PROBE | Peregrine Surgical , Ltd. | 2013-11-14 | 85 | 0 |
| K122997 | 23GA CURVED ILLUMINATING LASER PROBE | Peregrine Surgical , Ltd. | 2013-06-26 | 272 | 0 |
| K122905 | PEREGRINE 23GA CURVED LASER PROBE | Peregrine Surgical , Ltd. | 2013-04-30 | 221 | 0 |
| K061024 | PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60 | Peregrine Surgical , Ltd. | 2006-06-21 | 69 | 0 |
| K031023 | PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 | Peregrine Surgical , Ltd. | 2003-06-27 | 88 | 0 |
| K024061 | PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00 | Peregrine Surgical , Ltd. | 2003-03-07 | 88 | 0 |
| K990518 | PEREGRINE WET SET, MODEL PD400.00 | Peregrine Surgical , Ltd. | 1999-03-25 | 35 | 0 |
| K981907 | V.F.I.-VISCOUS FLUID INFUSION TUBING SET | Peregrine Surgical , Ltd. | 1998-08-04 | 64 | 0 |
| K980797 | PEREGRINE FIBER OPTIC MULTI-FUNCTION MANIPULATOR | Peregrine Surgical , Ltd. | 1998-05-19 | 78 | 0 |
| K980530 | PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, | Peregrine Surgical , Ltd. | 1998-05-12 | 90 | 0 |
| K980400 | PVRS-PEREGRINE VITREORETINAL SCISSOR MODEL PD505.10 | Peregrine Surgical , Ltd. | 1998-04-30 | 87 | 0 |
| K980399 | PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20 | Peregrine Surgical , Ltd. | 1998-04-30 | 87 | 0 |
| K980027 | PEREGRINE SHIELDED DIFFUSION PROBE | Peregrine Surgical , Ltd. | 1998-03-31 | 85 | 0 |
| K980025 | PEREGRINE TAPERED DIFFUSION PROBE | Peregrine Surgical , Ltd. | 1998-03-31 | 85 | 0 |
| K950529 | PEREGRINE DIFFUSION LIGHT PIPE | Peregrine Surgical , Ltd. | 1995-06-07 | 120 | 0 |
| K940393 | PEREGRINE WIDE ANGLE LIGHT PIPE | Peregrine Surgical , Ltd. | 1994-09-02 | 219 | 1 |
| K940392 | PEREGRINE PIC MINIPULATOR | Peregrine Surgical , Ltd. | 1994-08-23 | 209 | 0 |
| K940391 | PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE | Peregrine Surgical , Ltd. | 1994-06-08 | 133 | 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