Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of HeraeusLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Heraeus Lasersonics, Inc. with 38 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 1994: ULTRALINE II STERILE DISPOSABLE FIBER.
| Apr 21, 1994 | ULTRALINE II STERILE DISPOSABLE FIBERK933245 · GEX | 510(k) clearances |
| Nov 25, 1992 | HERCULES MODEL 5060 AND 5100 ND:YAG LASER SYSTEMSK923896 · GEX | 510(k) clearances |
| Jun 18, 1992 | ULTRALINE STERILE DISPOSABLE FIBERK921807 · GEX | 510(k) clearances |
| Jun 15, 1992 | ND;YAG SURGICAL LASER SYSTEMSK915578 · GEX | 510(k) clearances |
| Mar 27, 1992 | CO2 LASER AND WAVEGUIDE DELIVERY SYSTEMS FOR THOR.K915583 · GEX | 510(k) clearances |
| Feb 27, 1992 | LASER SYSTEMS FOR PERCUTANEOUS LUMBAR DISCECTOMYK912618 · GEX | 510(k) clearances |
| Dec 9, 1991 | C02 LASER WAVEGUIDEK913887 · GEX | 510(k) clearances |
| Oct 31, 1991 | CARBON DIOXIDE LASER SYSTEMS W/WAVEGUIDE DELIVERYK910530 · 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
