# Te ME NA S.A.R.L.

- Location (FDA's records): Oldsmar, FL
- FDA decisions: 7 (1999–2008): 7 510(k) clearances
- Names in FDA's records: Te ME NA S.A.R.L. (5); Te ME NA Sas (2)
- Product codes: BSP (2), BXN (1), CAZ (1), BSO (1), GXZ (1), FMF (1)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 22 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arrow Intl., Inc.: 1 (https://510kreport.com/company/arrow-intl)

## Firms that cite its devices most
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Its most-cited devices
- K080603: Hybrid Nerve Location Needle Coated and Uncoated (2008), cited by 1
- K991259: TE ME NA Epidural Catheter (2001), cited by 1
- K990100: Polymedic Upa Nerve Stimulation Needle; Polymedic Upc Nerve Stimulation Needle (2000), cited by 1

## Recent decisions
- K080603: Hybrid Nerve Location Needle Coated and Uncoated (Aug 5, 2008)
- K060186: Polyplex Stimulating Catheter System (Jul 18, 2006)
- K990323: TE ME NA Polystim Nerve Stimilator (Sep 28, 2001)
- K002405: Spinal Epidural Needles (Jun 1, 2001)
- K991259: TE ME NA Epidural Catheter (Feb 21, 2001)
- K990100: Polymedic Upa Nerve Stimulation Needle; Polymedic Upc Nerve Stimulation Needle (Aug 2, 2000)
- K990020: TE ME NA Loss of Resistance Syringe, 10CC (Jun 24, 1999)

Source page: https://510kreport.com/company/te-me-na