FDA Device Establishments · JSON-LD · Markdown

CORFLEX

FEI 1218997 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active

FEI Number1218997
Owner / OperatorCorflex Global, LLC (#1218997)
Address669 EAST INDUSTRIAL PARK, DRIVE, MANCHESTER, NH, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)ILI
Regulation § (21 CFR)890.3640
Proprietary namesSTRAP W/ VELSTRETCH AND LOOP LOC BLACK 2 X 22"; 8" COOLTEX THUMB SPICA W/ STRAP IFU; STRAP ANGLE CUT BLACK 1.5"X10"; LOOP 1"X1" WITH 1" LOOP LOC - BLACK; 2" X 2" LOW PROFILE HOOK TAB W DEADENED TIP; RANGER SHOULDER SLING; PADDED STRAP SLING XS; COLLAR & CUFF SLING; FACE STRAP WHITE 1.5 X 10.5" (12.5" overall length); SLING PADDED STRAP BLUE FOAM W/HOOK 40"

External sources

Source: openFDA. Public-domain (CC0).