FDA device listing

Air Lift Cushion,AIR LOCK CUSHIONS,Basic Foam Cushion w/LSII Cover,Basic Gel-Foam Cushion w/LSII Cover,CUSHION…

FDA device listing 1118232506 · SKIL-CARE CORP.

Key facts

Proprietary names Air Lift Cushion,AIR LOCK CUSHIONS,Basic Foam Cushion w/LSII Cover,Basic Gel-Foam Cushion w/LSII Cover,CUSHION, EMBROIDERED, FIBER FILLED,ECONO-GEL CUSHIONS,Foam Air Cushion,Gel-Foam Cushion,GEL FOAM TOILET SEAT CUSHION,Gel-Foam X Cushion,GEL-LIFT CUSHION,GEL-OVERLAY,Inflatable SquarePod Air Cushion,POSITION PLUS CUSHIONS,Premium Gel-Foam Cushion w/4-Way Cover,Stability Plus Cushion,THIN LINE GEL…
Owner/operator SKIL-CARE CORP.
Owner/operator number 2431497
Product codes KIC
Device names KIC - Cushion, Flotation
Device class Class I
Classification regulations (21 CFR) 890.3175
Review panels Physical Medicine
Registered establishments SKIL-CARE CORP.
Establishment registrations 2431497
FEI numbers 3000214954
Establishment operations Contract Manufacturer, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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