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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 50 of 65
DeviceModel / ReferenceRegistriesClassStatus
Extraction Spreader Size 1 2027-11A
EUDAMEDFDA UDI
Class IActive
Cheng Trephine 16mm 1426-12
EUDAMED
Class IActive
Cup Removal Starter Blade - 70mm 5205-70
EUDAMEDFDA UDI
Class IActive
Soft Tissue Shoulder Retractor 1260
EUDAMEDFDA UDI
Class IActive
Proximal Femoral Elevator Narrow with Standard Prongs 3420-05
EUDAMEDFDA UDI
Class IActive
Pin Inserter/Extractor 3030
EUDAMEDFDA UDI
Class IActive
Right Medial Retractor C1002
EUDAMEDFDA UDI
Class IActive
Grant TKA Anatomic Bone File Flat 6906-02
EUDAMEDFDA UDI
Class IActive
Anderson Talar Neck Osteotome 0.670 5075
EUDAMEDFDA UDI
Class IActive
Sm Bone Comp/Dist 1/16" w/Ro Arms w/o Driver & Case 1825-01-05
EUDAMEDFDA UDI
Class IActive
Cup Removal Finish Instrument - 60mm 5201-60
EUDAMEDFDA UDI
Class IActive
Stanton Straight Pin Removal Pliers 1893
EUDAMEDFDA UDI
Class IActive
3/32 mm x 6" Pin with Suture Hole 1227
EUDAMEDFDA UDI
Class IActive
Superior Capsular Retractor 7140
EUDAMEDFDA UDI
Class IActive
Lee Pin Adjustment Guide 1.1mm/1.6mm 3013-01
EUDAMEDFDA UDI
Class IActive
Kolbel Self-Retaining Retractor Blade 20mm x 36mm Each T1022
EUDAMEDFDA UDI
Class IActive
Hip Cup Wrench Finish Blade - 54mm Exchange 5206W-54
EUDAMEDFDA UDI
Class IActive
Offset Long Curette Size 00 5060-01
EUDAMEDFDA UDI
Class IActive
Meyer Latarjet Forceps Small 5257-01
EUDAMEDFDA UDI
Class IActive
Nordt Micro Fracture Set 8025-00
EUDAMEDFDA UDI
Class IActive
Lachiewicz Angled Femoral Component Disimpactor Exchange 3700-03-E
EUDAMEDFDA UDI
Class IActive
13mm x 8mm Impactor Tip Oval Steel 5370-02
EUDAMEDFDA UDI
Class IActive
Guide 8093-00
EUDAMEDFDA UDI
Class IActive
Chung Weitlaner Retractor 2x3 Prongs Blunt Tips 30mm 5067
EUDAMEDFDA UDI
Class IActive
McKinley Foraminal Probe Extra Large 6mm/0.196" 5001-XL
EUDAMED
Class IActive
Cup Removal Finish Blade - 48mm 5206-48
EUDAMEDFDA UDI
Class IActive
Curved Hohmann Retractor Wide 6215
EUDAMEDFDA UDI
Class IActive
Modified Curved Double Bent Hohmann Retractor D6107-MOD
EUDAMEDFDA UDI
Class IActive
Curved Anterior Retractor Wide, Deep 7804-03D
EUDAMEDFDA UDI
Class IActive
Mazzara Rongeur 2x10mm Bite with Small Pistol Grip Handle 1765-04
EUDAMEDFDA UDI
Class IActive
Universal Hip Extractor Repair Kit 3610-KIT
EUDAMEDFDA UDI
Class IActive
Gupta T-Handle Spine Probe Flat Tip 5005-03
EUDAMEDFDA UDI
Class IActive
Modified Smith-Peterson Style Osteotome Extra Long 5280-04
EUDAMEDFDA UDI
Class IActive
Unger Total Knee Revision Osteotome Starter Wide 4701
EUDAMEDFDA UDI
Class IActive
Extension 4" (4" Spacer with 6" Knob) 4150-EXT4
EUDAMEDFDA UDI
Class IActive
Mobile Body Assembly Knurled Thumb Screw 7447-01-03
EUDAMEDFDA UDI
Class IActive
Duke Enhanced Cement Remover 5229
EUDAMEDFDA UDI
Class IActive
Collateral Ligament Retractor 6620
EUDAMEDFDA UDI
Class IActive
MIH Small Hohmann Retractor S3030
EUDAMEDFDA UDI
Class IActive
Posterior/Inferior Retractor Medium Left 7925-02
EUDAMEDFDA UDI
Class IActive
Bonney Tissue Forceps 10" with Teeth 5040
EUDAMEDFDA UDI
Class IActive
Glenoid Spreader with Forked/Disc Ends Left 1861-L
EUDAMEDFDA UDI
Class IActive
Moran Acetabular Retractor Left 6415-L
EUDAMEDFDA UDI
Class IActive
Weinraub Joint & Calcaneal Spreader 2.8mm Pin Dia 1872
EUDAMEDFDA UDI
Class IActive
Femoral Guide RR1388
EUDAMEDFDA UDI
Class IActive
Universal Joint with Quick Connect 2027-04
EUDAMEDFDA UDI
Class IActive
Tissue Grasper Angled Down with Shark Teeth Small 7" 1784-03
EUDAMEDFDA UDI
Class IActive
Wiater Shoulder Bone Hook 5079
EUDAMEDFDA UDI
Class IActive
Double Bent Hohmann Retractor Extra Long 3" Blade 6210-04
EUDAMEDFDA UDI
Class IActive
Ortholucent Small Bone Clamp 1828
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.