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Innomed, Inc.

United States·US-MF-000014761

Last updated September 17, 2026

Information

Country
United States
Address
103, Estus Drive, Savannah, United States
LinkedIn
—
Facebook
—
Phone
+1 912 236 0000
PRRC Contact
Aaron Ingram
EUDAMED SRN
US-MF-000014761
FDA FEI Number
1833053
DUNS Number
878427491

Catalogue (3242)

Page 19 of 65
DeviceModel / ReferenceRegistriesClassStatus
Stanton Reverse Ragnell Retractor Deep 4510-02
EUDAMEDFDA UDI
Class IActive
Chung Weitlaner Retractor 2x3 Prongs Sharp Tips 25mm 5066
EUDAMEDFDA UDI
Class IActive
Coated Modified Proximal Femoral Elevator 3420-06
EUDAMEDFDA UDI
Class IActive
SS Ratchet Frame w/Ortholucent Arms & Blades Set 7428-00
EUDAMEDFDA UDI
Class IActive
Curved Canal Rasp 12mm 3004-01-12
EUDAMEDFDA UDI
Class IActive
Ortho Mini Gouge 8mm 1168-8
EUDAMEDFDA UDI
Class IActive
Lombardi Femoral Tibial Spreader Large w/Lock Ratchet 1875-LR
EUDAMEDFDA UDI
Class IActive
Posterior Support Pad 4170-PP
EUDAMEDFDA UDI
Class IActive
Radiolucent Peg 6" 4090-06
EUDAMEDFDA UDI
Class IActive
Left Inferior Posterior Acetabular Retractor C1007
EUDAMEDFDA UDI
Class IActive
9" Intraarticular Tissue Grasper/Rongeur Small Grip Handle 1790-02-SG
EUDAMEDFDA UDI
Class IActive
Mazzara Rongeur 4x10mm Bite with Small Pistol Grip Handle 1765-05
EUDAMEDFDA UDI
Class IActive
McGlamry Type Elevator 15mm 1543-15
EUDAMEDFDA UDI
Class IActive
Wixson/Stulberg Anterior Support Retaining Collar Half 4110-E
EUDAMEDFDA UDI
Class IActive
Modified Smith-Peterson Style Osteotome Medium 5280-02
EUDAMEDFDA UDI
Class IActive
5-Prong Rake Blade 7450-10B
EUDAMEDFDA UDI
Class IActive
Goytia Stackable Hohmann Retractor Deep 4551-D
EUDAMEDFDA UDI
Class IActive
Kopplin Pain Catheter Insertion Grasperq 1783
EUDAMEDFDA UDI
Class IActive
Double Bent Hohmann Acetabular Retractor 2.5" Blade 6210
EUDAMEDFDA UDI
Class IActive
Stanton Distal Hum Fem Tib Nail/Screw Lock Guide Assembly 8986-00
EUDAMEDFDA UDI
Class IActive
Browne Deltoid Retractor Small Deep 1670-01D
EUDAMEDFDA UDI
Class IActive
Narrow Modified Fukuda Type Retractor 1930
EUDAMEDFDA UDI
Class IActive
Z Knee Retractor Large 4420-01
EUDAMED
Class IActive
Joint Calcaneal Distractor Small Closed Arms 4210-SS
EUDAMEDFDA UDI
Class IActive
Superior Retractor 6027
EUDAMEDFDA UDI
Class IActive
Kolbel Self-Retaining Glenoid Retractor Set T1014
EUDAMEDFDA UDI
Class IActive
Deep Flared Fukuda Type Retractor with Spikes 1905-D
EUDAMEDFDA UDI
Class IActive
Alvi Three Inch Tapered Blade 7425-03
EUDAMEDFDA UDI
Class IActive
Cobra Retractor Ortholucent Standard 6130-R
EUDAMEDFDA UDI
Class IActive
Hook Cup Extractor 6.5mm without Slaphammer 3660-01
EUDAMEDFDA UDI
Class IActive
Adjustable Hip Rest Assembly Arm Bar with Knob 4030-A
EUDAMEDFDA UDI
Class IActive
Sanders Femoral Neck Cutting Block 5 x 10mm 4555
EUDAMEDFDA UDI
Class IActive
Incavo Tibial Component Revision Osteotome Standard 3621-01
EUDAMEDFDA UDI
Class IActive
Connelly Leg Positioning Board 2626-01
EUDAMEDFDA UDI
Class IActive
Lombardi 12/14mm Taper Cleaner 8035-02
EUDAMEDFDA UDI
Class IActive
Hip Cup Wrench Finish Blade - 76mm Exchange 5206W-76
EUDAMEDFDA UDI
Class IActive
Sterilized Disposable Footpiece Liner (10 per Case) 2629-00
EUDAMEDFDA UDI
Class IActive
Cup Removal Finish Blade - 56mm 5206-56
EUDAMEDFDA UDI
Class IActive
Retractor ME-EC0007 ME-EC0007
EUDAMEDFDA UDI
Class IActive
Ambidexterous Self Retaining Retractor with 4 Teeth 1579
EUDAMEDFDA UDI
Class IActive
Starting/Finishing Case Lid Inventory 9015-LI
EUDAMEDFDA UDI
Class IActive
Bhargava DAA Femoral Stem Impactor 5308
EUDAMEDFDA UDI
Class IActive
Booth Knee Retractor 6580
EUDAMEDFDA UDI
Class IActive
Durham Leg Positioner Pad 4105-P
EUDAMEDFDA UDI
Class IActive
Lachiewicz Cement Hook 8mm Wide 3700-10
EUDAMEDFDA UDI
Class IActive
Auerbach Hand Plate 1747-01
EUDAMEDFDA UDI
Class IActive
Wrench Drive Finish Cup Cutter - 54mm 5209-54
EUDAMEDFDA UDI
Class IActive
Anterior Upright Support 4170-03
EUDAMEDFDA UDI
Class IActive
Arm Board 2419
EUDAMEDFDA UDI
Class IActive
Eickmann Revision Chisel 8mm Exchange 5470-08-E
EUDAMEDFDA UDI
Class IActive

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Mar 7, 2024Z-1753-2024—completed

54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.