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ORTHO DEVELOPMENT CORP.

Last updated September 17, 2026

Information

Country: US
Address: 12187 SOUTH BUSINESS PARK DR., DRAPER, UT, 84020
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000143502
DUNS Number: —

Catalogue (3843)

Page 2 of 77

Device	Model / Reference	Registries	Class	Status
Pagoda	752-4535-12	FDA UDI	Class II	Unknown
Vusion OS	551-7309	FDA UDI	Class II	Unknown
Vusion TS	551-1008	FDA UDI	Class II	Unknown
Ibis	158-1035-03A	FDA UDI	Class II	Active
Balanced Knee System	163-2314	FDA UDI	Class II	Active
Balanced Knee System	161-1504	FDA UDI	Class II	Active
Vusion CS Plus	159-1608-00A	FDA UDI	Class II	Active
BKS E-Vitalize	166-7414	FDA UDI	Class II	Active
Balanced Knee System	163-3716	FDA UDI	Class II	Active
Integrated Spine System	158-6560-01	FDA UDI	Class II	Unknown
Ovation Hip Stem	101-0009	FDA UDI	Class II	Active
BKS E-Vitalize	166-7112	FDA UDI	Class II	Active
Legend	175-4054	FDA UDI	Class II	Active
BKS® Uni	763-6101A	FDA UDI	Class II	Active
Balanced Knee System Revision	567-7206A	FDA UDI	Class II	Active
Pagoda	158-3045-01A	FDA UDI	Class II	Active
Legend	174-2848	FDA UDI	Class II	Active
Balanced Knee System	163-1418	FDA UDI	Class II	Active
Ibis	752-8560-41	FDA UDI	Class II	Unknown
BKS TriMax PS Plus	166-8418	FDA UDI	Class II	Active
Legend	173-3260	FDA UDI	Class II	Active
Vusion CS Plus	159-1610-07A	FDA UDI	Class II	Active
Solitude Unipolar	132-0042	FDA UDI	Class II	Active
Balanced Knee System	163-1113	FDA UDI	Class II	Active
Pivot Bipolar	133-2248	FDA UDI	Class II	Active
Solitude Unipolar	132-0038	FDA UDI	Class II	Active
Pagoda	158-3030-01	FDA UDI	Class II	Unknown
Vusion OS	551-6108A	FDA UDI	Class II	Active
Balance Knee Revision System	563-1610	FDA UDI	Class II	Active
Escalade Acetabular System	170-0366	FDA UDI	Class II	Active
Tri-plus	138-3209	FDA UDI	Class II	Active
Solitude Unipolar	132-1230	FDA UDI	Class II	Active
Balance Knee Revision System	567-6105	FDA UDI	Class II	Active
Integrated Spine System	158-0120	FDA UDI	Class II	Unknown
BKS® Uni	763-2102A	FDA UDI	Class II	Active
Balance Knee Revision System	566-1511	FDA UDI	Class II	Active
Legend Acetabular Shell	170-0456	FDA UDI	Class II	Active
Balanced Knee System	163-5613	FDA UDI	Class II	Active
Vusion CS Plus	159-1212-07	FDA UDI	Class II	Unknown
Envision	154-5122	FDA UDI	Class II	Unknown
Balanced Knee System	163-3114	FDA UDI	Class II	Active
Balance Knee Revision System	561-1402	FDA UDI	Class II	Active
BKS® Uni	763-1101A	FDA UDI	Class II	Active
Balanced Knee System	161-1103A	FDA UDI	Class II	Active
Balanced Knee System	161-3501A	FDA UDI	Class II	Active
Balance Knee Revision System	563-1130	FDA UDI	Class II	Active
Balance Knee Revision System	562-1100	FDA UDI	Class II	Active
Legend	175-2842	FDA UDI	Class II	Active
Alpine	700-0315	FDA UDI	Class II	Active
Balanced Knee Revision System	561-5258	FDA UDI	Class II	Active

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FDA Recalls (28)

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

Date	Recall No.	Class	Status	Reason
May 30, 2019	Z-1903-2020	—	open, classified	The locking mechanism of the tibial tray exhibited a manufacturing defect in which a uniform ridge was cut along the inner wall of the "T" and "Y" junctions, which may cause resistance when the Tibial Insert was being assembled.
May 30, 2019	Z-1904-2020	—	open, classified	The locking mechanism of the tibial tray exhibited a manufacturing defect in which a uniform ridge was cut along the inner wall of the "T" and "Y" junctions, which may cause resistance when the Tibial Insert was being assembled.
Jul 11, 2014	Z-2257-2014	—	terminated	Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not properly seal, allowing air to seep back into the pouch after sealing which increases the risk that the material properties of the implant would be substantially degraded due to oxidation.
Jul 11, 2014	Z-2256-2014	—	terminated	Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not properly seal, allowing air to seep back into the pouch after sealing which increases the risk that the material properties of the implant would be substantially degraded due to oxidation.
Jul 11, 2014	Z-2255-2014	—	terminated	Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not properly seal, allowing air to seep back into the pouch after sealing which increases the risk that the material properties of the implant would be substantially degraded due to oxidation.
Jul 11, 2014	Z-2253-2014	—	terminated	Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not properly seal, allowing air to seep back into the pouch after sealing which increases the risk that the material properties of the implant would be substantially degraded due to oxidation.
Jul 11, 2014	Z-2254-2014	—	terminated	Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not properly seal, allowing air to seep back into the pouch after sealing which increases the risk that the material properties of the implant would be substantially degraded due to oxidation.
Apr 1, 2014	Z-1610-2014	—	terminated	A femoral component containing pegs was found in a box for the pegless version.
Dec 19, 2011	Z-0740-2012	—	terminated	Tip of hex-head screwdriver may break off during use in hip replacement procedure.
May 10, 2011	Z-2602-2011	—	terminated	Tests on PVC packaging material resulted in alert levels for cytotoxicity.
May 10, 2011	Z-2603-2011	—	terminated	Tests on PVC packaging material resulted in alert levels for cytotoxicity.
Jan 11, 2011	Z-1673-2011	—	terminated	Component of total hip arthroplasty may break during surgical procedure.
Jan 11, 2011	Z-1670-2011	—	terminated	Component of total hip arthroplasty may break during surgical procedure.
Jan 11, 2011	Z-1671-2011	—	terminated	Component of total hip arthroplasty may break during surgical procedure.
Jan 11, 2011	Z-1672-2011	—	terminated	Component of total hip arthroplasty may break during surgical procedure.
Jan 7, 2011	Z-1740-2011	—	terminated	Components of a replacement knee system could be mislabeled.
Jan 7, 2011	Z-1741-2011	—	terminated	Components of a replacement knee system could be mislabeled.
Jan 7, 2011	Z-1742-2011	—	terminated	Components of a replacement knee system could be mislabeled.
Jul 28, 2010	Z-0315-2011	—	terminated	The hip stem did not fit the distal centralizer because the hole was not drilled with the appropriate taper.
May 29, 2009	Z-1993-2009	—	terminated	Erroneous lot number on 3 of 28 units of Balanced Knee System. Three units from Lot Number 0055245 were mixed in with the recalled lot (0054891).
Apr 29, 2009	Z-0086-2010	—	terminated	A Pivot BiPolar Head, the femoral head in a hip prosthesis, might not move freely after assembly due a stacking up of manufacturing tolerances.
Mar 19, 2009	Z-1229-2010	—	terminated	A component of knee prosthesis was assembled incorrectly.
Mar 19, 2009	Z-1228-2010	—	terminated	A component of knee prosthesis was assembled incorrectly.
Sep 15, 2003	Z-0042-04	—	terminated	The guide pin which rotationally constrains the tibial punch within the punch guide, may fall out.
Dec 26, 2002	Z-0567-03	—	terminated	Cleaning agent residue from packaging material was adhering to implantable hip stems.
Dec 26, 2002	Z-0568-03	—	terminated	Cleaning agent residue from packaging material was adhering to implantable hip stems.
Dec 26, 2002	Z-0566-03	—	terminated	Cleaning agent residue from packaging material was adhering to implantable hip stems.
Dec 26, 2002	Z-0569-03	—	terminated	Cleaning agent residue from packaging material was adhering to implantable hip stems.