
The Telos Co.
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THE TELOS EQUIPMENT is an FDA 510(k)-cleared medical device (K812778) manufactured by The Telos Co.. This device is classified under the Orthopedic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 7, 1981. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057