Medical device makerLabelled 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 Influence with 16 510(k) clearances. The most recent is a 510(k) clearance dated Aug 27, 1999: REPOSE BONE SCREW SYSTEM.
| Aug 27, 1999 | REPOSE BONE SCREW SYSTEMK981677 · LRK | 510(k) clearances |
| Aug 12, 1999 | CRYO-MONO CRYOGENIC SYSTEM, MODEL CRYO-MONO WITH TUF PROBEK991792 · GEH | 510(k) clearances |
| Jul 30, 1999 | STAPLETAC BONE ANCHOR SYSTEMK992277 · HWC | 510(k) clearances |
| Jul 1, 1999 | CRYO-MONO CRYOGRNIC SYSTEMK991122 · GEH | 510(k) clearances |
| Feb 16, 1999 | MICROTAC-BONE ANCHOR SYSTEMK990160 · MBI | 510(k) clearances |
| Feb 1, 1999 | STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEMK990095 · MBI | 510(k) clearances |
| Nov 24, 1998 | IN-PROBE II URODYNAMIC SYSTEMK983325 · FEN | 510(k) clearances |
| Aug 31, 1998 | SHORT STRAIGHT-IN BONE SCREW FIXATION SYSTEMK982155 · MBI | 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
