SPAN-AMERICA MEDICAL SYSTEMS, INC.

FDA Device Registration & Listing · GREENVILLE, SC, US · Registration 1041130

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1041130
FEI Number
1041130
Entity Name
SPAN-AMERICA MEDICAL SYSTEMS, INC.
City/State/Country
GREENVILLE, SC, US
Establishment Address
70 Commerce Ctr, GREENVILLE, SC 29615, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Savaria Corporation (Owner Number: 1041130)
Owner / Operator Contact Address
70 Commerce Center, Greenville, SC 29615, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SPAN+AIDS COCK-UP SPLINT SPAN+AIDS TABLE PILLOW SPAN+AIDS SCHAEFER ABDUCTION PILLOW SPAN+AIDS THORACOTO SPAN+AIDS CAST ELEVATOR SPA+AIDS ANKLET SPAN+AIDS TROCHANTER WEDGE SPAN+AIDS CRADLE BOOT HEEL PILLOW SPA+AIDS WRISTLET SPAN+AIDS SAFETY STRAP SPAN-AIDS OR HEAD POSITIONER O.R. DONUT BODY ALIGNER ULNAR NERVE PROTECTOR LAMINECTOMY ARM CRADLES CAST ELEVATOR MULTI-CRADLE POSITIONER SPAN+AIDS ABDUCTION PILLOW SPAN+AIDS WRIST RESTRAINT SPAN+AIDS LAMINECTOMY ARM CRADLE SPAN+AID BRIDGING PILLOW SYSTEM SPAN+AIDS FOOT DROP STOP SPAN+AIDS OPEN HEART SURGERY KIT SPAN+AIDS WHEELCHAIR WEDGE SPAN+AIDS FACE SPAN+AIDS PT PRONE PILLOW SPANHAIDS BODY ALIGNER SPAN+AIDS HEAD CRADLE Risk Manager SHOULDER ABDUCTION POSITIONERS ABDUCTION PILLOWS Silvalea Slings Span America SURGICAL TABLE CUSHION Convoluted Foam Overylay GEOMATTRESS COVER PRESSUREGUARD COVER Head Cradle Convoluted Overlay Convoluted cushion Donut Wedge GEO-MATT Sacral Pads Heel Protector Elbow Protector O.R. Armboard Pads GEL ARMBOARD PAD GEL TABLE PAD CRADLE BOOTS ULNAR NERVE PROTECTOR FOOT DROP STOPS CUSTOM CARE THE TOPPER GEO-MATTRESS HC MAX PRO PLUS ATLAS PG RENEW ULTRA MAX STRETCHER GULF SOUTH SELECT SOLUTION ULTRA MAX WINGS GEO-MATTRESS GEOMATT WHEELCHAIR CUSHION GEOMATT CONTOUR ISCH DISH SHORT WAVE CROSS CUT EZ-DISH EQUALIZER GEO WAVE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCX Support, Patient Position Anesthesiology Class 1 868.6820 1992-07-08
IKX Aid, Transfer Physical Medicine Class 1 890.5050 2009-02-18
IOZ Splint, Abduction, Congenital Hip Dislocation Physical Medicine Class 1 890.3665 2012-11-06
IOY Support, Arm Physical Medicine Class 1 890.3475 2012-11-06
INE Sling, Overhead Suspension, Wheelchair Physical Medicine Class 1 890.3910 2019-07-23
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2018-05-25
LWG Surgical Table Cushion General, Plastic Surgery Class 1 878.4950 1997-06-13
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2012-11-06
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 1997-05-23
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 1995-10-02
IMP Cushion, Wheelchair Physical Medicine Class 1 890.3920 1992-07-08

Official Correspondent

Erika Ramsbottom

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Savaria Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3013169808 Savaria Concord Lifts, Inc. Magog Quebec, CA
8022290 SPAN MEDICAL PRODUCTS CANADA ULC BEAMSVILLE Ontario, CA

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2018 Handicare Usa Inc 1
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018 Handicare AB Maskinvagen 1
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1041130. Last updated year: 2026. Please use registration number 1041130 when referencing this establishment in official correspondence.
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