FDA Device Establishments · JSON-LD · Markdown

Nutec Rehab Inc.

FEI 3000161972 · Manufacture Medical Device · Status: Active

FEI Number3000161972
Owner / OperatorNutec Rehab Inc. (#10058512)
Address5840 S Watt Ave Ste A, SACRAMENTO, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KNO
Regulation § (21 CFR)890.3910
Proprietary namesNT-DH288 - Nutec 2" Drop Hook - 1" Tubing; Nutec Rehab, Inc.; NT-K-FH78 - Nutec Flush Mount Kit 7/8"; HR-HRAP - Nutec Headrest Adapter Plate; NT-FB001 - Nutec Flat Bracket Assembly; FB-DLM - Nutec Double Leg Foot Boxes - Medium; NT-K-DH388 - Nutec 3" Drop Hook Kit with Stops - 1" Tubing; HR-CPAD-L - Nutec Concave Headrest Pad Large; PB-BFM - Nutec Butterfly Chest Belt - Medium; NT-DH001 - Nutec 1" Drop Hook Assembly"

External sources

Source: openFDA. Public-domain (CC0).