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 Te ME NA S.A.R.L. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 5, 2008: HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED.
| Aug 5, 2008 | HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATEDK080603 · BSP | 510(k) clearances |
| Jul 18, 2006 | POLYPLEX STIMULATING CATHETER SYSTEMK060186 · CAZ | 510(k) clearances |
| Sep 28, 2001 | TE ME NA POLYSTIM NERVE STIMILATORK990323 · BXN | 510(k) clearances |
| Jun 1, 2001 | SPINAL EPIDURAL NEEDLESK002405 · BSP | 510(k) clearances |
| Feb 21, 2001 | TE ME NA EPIDURAL CATHETERK991259 · BSO | 510(k) clearances |
| Aug 2, 2000 | POLYMEDIC UPA NERVE STIMULATION NEEDLE; POLYMEDIC UPC NERVE STIMULATION NEEDLEK990100 · GXZ | 510(k) clearances |
| Jun 24, 1999 | TE ME NA LOSS OF RESISTANCE SYRINGE, 10CCK990020 · FMF | 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
