Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Peregrine Surgical with 20 510(k) clearances. The most recent is a 510(k) clearance dated Aug 5, 2024: Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfie….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 5, 2024 | Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)K233653 · MPA | 510(k) clearances |
| Sep 11, 2015 | 23ga Chandelier Illuminator, 25ga Chandelier IlluminatorK151604 · MPA | 510(k) clearances |
| Nov 14, 2013 | PEREGRINE CURVED ILLUMINATING LASER PROBEK132614 · HQB | 510(k) clearances |
| Jun 26, 2013 | 23GA CURVED ILLUMINATING LASER PROBEK122997 · HQB | 510(k) clearances |
| Apr 30, 2013 | PEREGRINE 23GA CURVED LASER PROBEK122905 · HQB | 510(k) clearances |
| Jun 21, 2006 | PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60K061024 · HQF | 510(k) clearances |
| Jun 27, 2003 | PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10K031023 · HQF | 510(k) clearances |
| Mar 7, 2003 | PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00K024061 · GEX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
