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 13, 2026, FDA's public records list Laser Peripherals with 12 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jun 8, 2017: Laser Peripherals, LLC Family of Bare Laser Fibers.
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.
| Date | Record | Source |
|---|---|---|
| Jun 8, 2017 | Laser Peripherals, LLC Family of Bare Laser FibersK170366 · GEX | 510(k) clearances |
| Jun 20, 2014 | LP,Surgical Fibers, Bare Laser Fiber 600 micron, DBLF-60-2, Sterile EO. Laser surgical instrument for use in general and plastic surgeryClass II · Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling that indicated a sterility expiration dat | Device recalls |
| Apr 25, 2003 | BARE LASER FIBER MODELS DBLF-40, DBLF-60, DBLF-60-1, DCLF-600B, DSLF-60, DBLF-100K030959 · GEX | 510(k) clearances |
| Jul 24, 2001 | LASER PERIPHERALS REUSABLE HOLMIUM FIBERK011207 · GEX | 510(k) clearances |
| Jul 12, 1999 | SCATTERFREE LATERAL EMITTING FIBERK992083 · GEX | 510(k) clearances |
| Feb 10, 1998 | LS-905 FIBERCHOICE ADAPTER SYSTEMK974229 · GEX | 510(k) clearances |
| Jul 29, 1997 | LASER PERIPHERALS HOLMIUM BARE FIBERSK972272 · GEX | 510(k) clearances |
| Jun 27, 1996 | LASER PERIPHERALS INC. BARE FIBERK961516 · GEX | 510(k) clearances |
| May 22, 1996 | LASER PERIPHERALS INC. SCATTERFREE FIBERK961079 · 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
