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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 5 of 77

Device	Model / Reference	Registries	Class	Status
Pisces Spinal System	753-8540-20	FDA UDI	Class II	Active
Vusion CS Plus	159-1410-00A	FDA UDI	Class II	Active
BKS E-Vitalize	166-7318	FDA UDI	Class II	Active
Vusion OS	551-7308A	FDA UDI	Class II	Active
BKS® Uni	763-2061	FDA UDI	Class II	Active
Vusion CS Plus	159-1409-00A	FDA UDI	Class II	Active
BKS E-Vitalize	166-6214	FDA UDI	Class II	Active
Balanced Knee System	163-5408	FDA UDI	Class II	Active
Pagoda	158-3085-01	FDA UDI	Class II	Unknown
BKS E-Vitalize	166-5420	FDA UDI	Class II	Active
BKS® Uni	762-1200	FDA UDI	Class II	Active
Entrada Hip Stem	510-1221	FDA UDI	Class II	Active
Ibis	752-4530-26	FDA UDI	Class II	Unknown
Alpine	700-0210A	FDA UDI	Class II	Active
Escalade Acetabular System	171-3260	FDA UDI	Class II	Active
Balanced Knee System	163-1516	FDA UDI	Class II	Active
Balance Knee Revision System	568-1504	FDA UDI	Class II	Active
Vusion OS	551-7211	FDA UDI	Class II	Unknown
BKS E-Vitalize	166-5114	FDA UDI	Class II	Active
Legend	174-3246	FDA UDI	Class II	Active
Balanced Knee System	163-3707	FDA UDI	Class II	Active
BKS® Uni	761-1301	FDA UDI	Class II	Active
Delta Ceramic Femoral Head	136-3660	FDA UDI	Class II	Active
BKS® Uni	763-8101A	FDA UDI	Class II	Active
Balanced Knee System	161-1502A	FDA UDI	Class II	Active
Ibis	752-4525-26A	FDA UDI	Class II	Active
CoCr Femoral Head	138-4090	FDA UDI	Class II	Active
Balance Knee Revision System	562-2400	FDA UDI	Class II	Active
BKS® Uni	761-1201	FDA UDI	Class II	Active
BKS® Uni	762-4200	FDA UDI	Class II	Active
Delta Ceramic Femoral Head	136-4013	FDA UDI	Class II	Active
Balanced Knee System	163-2210	FDA UDI	Class II	Active
Balanced Knee System	161-1203	FDA UDI	Class II	Active
Balanced Knee System	163-1511	FDA UDI	Class II	Active
Balanced Knee Revision System	563-2512	FDA UDI	Class II	Active
Pisces Spinal System	753-4525-10A	FDA UDI	Class II	Active
Integrated Spine System	158-7535-01	FDA UDI	Class II	Unknown
BKS E-Vitalize	166-6407	FDA UDI	Class II	Active
Vusion OS	551-7112	FDA UDI	Class II	Unknown
Balanced Knee System	161-1303	FDA UDI	Class II	Active
Balanced Knee System	161-2402	FDA UDI	Class II	Active
BKS E-Vitalize	166-5411	FDA UDI	Class II	Active
Vusion TS	551-5016A	FDA UDI	Class II	Active
BKS E-Vitalize	166-5710	FDA UDI	Class II	Active
Pagoda	158-3075-01A	FDA UDI	Class II	Active
Legend	174-4058	FDA UDI	Class II	Active
BKS E-Vitalize	166-6611	FDA UDI	Class II	Active
Ibis	158-0040-03	FDA UDI	Class II	Unknown
Vusion OS	551-6409A	FDA UDI	Class II	Active
Pagoda	752-6555-11A	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.