SEARCH RESULTS FOR: (*Imitation St. Paul*)(16330 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ST Internal Fixture - 08806388236817

Ø4/ L=11.5
Megagen Implant Co. Ltd
ST4011
In Commercial Distribution

  • 08806388236817 ()
ST4011C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236800

Ø4/ L=10
Megagen Implant Co. Ltd
ST4010
In Commercial Distribution

  • 08806388236800 ()
ST4010C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236794

Ø4/ L=8.5
Megagen Implant Co. Ltd
ST4008
In Commercial Distribution

  • 08806388236794 ()
ST4008C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236787

Ø4/ L=7
Megagen Implant Co. Ltd
ST4007
In Commercial Distribution

  • 08806388236787 ()
ST4007C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236770

Ø3.5/ L=15
Megagen Implant Co. Ltd
ST3515
In Commercial Distribution

  • 08806388236770 ()
ST3515C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236763

Ø3.5/ L=13
Megagen Implant Co. Ltd
ST3513
In Commercial Distribution

  • 08806388236763 ()
ST3513C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236756

Ø3.5/ L=11.5
Megagen Implant Co. Ltd
ST3511
In Commercial Distribution

  • 08806388236756 ()
ST3511C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236749

Ø3.5/ L=10
Megagen Implant Co. Ltd
ST3510
In Commercial Distribution

  • 08806388236749 ()
ST3510C

  • Screw endosteal dental implant, two-piece

ST Internal Fixture - 08806388236732

Ø3.5/ L=8.5
Megagen Implant Co. Ltd
ST3508
In Commercial Distribution

  • 08806388236732 ()
ST3508C

  • Screw endosteal dental implant, two-piece

TETRIS ST 20° - 04047844114254

The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution

  • 04047844114254 ()

  • 17x10x32mm
TST20171032

  • Metallic spinal interbody fusion cage
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