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 Smith & NephewLabelled by claude-sonnet-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 15, 2026, FDA's public records list Oratec Interventions, Inc. with 24 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 2002: NUCLEOTOMY INTRADISCAL CATHETER.
| Jan 31, 2002 | NUCLEOTOMY INTRADISCAL CATHETERK013622 · GEI | 510(k) clearances |
| Aug 29, 2001 | VULCAN TAC PROBES, MODEL 911XXXK003198 · HRX | 510(k) clearances |
| Mar 1, 2001 | VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300XK003893 · HRX | 510(k) clearances |
| May 4, 2000 | VULCAN ELECTROSURGICAL PROBES: VULCAN MICRO LIGAMENT CHISELS, VULCAN LIGAMENT CHISELS, VULCAN EFLEX LIGAMENT CHISELSK000691 · HRX | 510(k) clearances |
| Feb 4, 2000 | ORATEC ABLATOR-S PROBES (MONOPOLAR ABLATION SUCTION PROBES)K992805 · GEI | 510(k) clearances |
| Jan 18, 2000 | ORA-50 ELECTROTHERMAL SYSTEM AND ACCESSORIESK994333 · GEI | 510(k) clearances |
| Dec 17, 1999 | ORATEC SPINECATH INTRADISCAL CATHETER, MODEL 920002K993967 · GEI | 510(k) clearances |
| Dec 6, 1999 | ORA-50 S AUTOTEMP ELECTROTHERMAL SPINE SYSTEM AND ACCESSORIESK993854 · GEI | 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
