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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: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000143502
DUNS Number: —

Catalogue (3843)

Page 10 of 77

Device	Model / Reference	Registries	Class	Status
Balanced Knee System	161-1305	FDA UDI	Class II	Active
Biolox Delta	136-3603	FDA UDI	Class II	Active
Vusion PS	551-5315	FDA UDI	Class II	Unknown
Balanced Knee System Revision	568-1412A	FDA UDI	Class II	Active
Ibis	752-5545-21	FDA UDI	Class II	Unknown
Surespace	SST2070	FDA UDI	Class II	Active
BKS E-Vitalize	166-6218	FDA UDI	Class II	Active
Pagoda	752-7590-31A	FDA UDI	Class II	Active
BKS® Uni	763-2062A	FDA UDI	Class II	Active
Balance Knee Revision System	567-2206	FDA UDI	Class II	Active
BKS E-Vitalize	166-5109	FDA UDI	Class II	Active
Balanced Knee System	161-3402	FDA UDI	Class II	Active
Trivicta	513-1008	FDA UDI	Class II	Active
Balanced Knee System	161-1604	FDA UDI	Class II	Active
Escalade Acetabular System	171-3254	FDA UDI	Class II	Active
Balance Knee Revision System	563-1514	FDA UDI	Class II	Active
Legend Acetabular Shell	170-0654	FDA UDI	Class II	Active
Vusion OS	551-6212	FDA UDI	Class II	Unknown
Balanced Knee System	163-1416	FDA UDI	Class II	Active
BKS TriMax PS Plus	166-8416	FDA UDI	Class II	Active
Balanced Knee System	163-2310	FDA UDI	Class II	Active
Pagoda	158-0090-01A	FDA UDI	Class II	Active
Vusion OS	551-7612	FDA UDI	Class II	Unknown
Balanced Knee System	163-2209	FDA UDI	Class II	Active
BKS® Uni	763-3101A	FDA UDI	Class II	Active
Vusion CS Plus	159-1207-07	FDA UDI	Class II	Unknown
Vusion CS Plus	159-1411-07A	FDA UDI	Class II	Active
Legend	172-2850	FDA UDI	Class II	Active
Vusion OS	551-7110	FDA UDI	Class II	Unknown
Vusion OS	551-6111A	FDA UDI	Class II	Active
Entrada Hip Stem	510-0210	FDA UDI	Class II	Active
Pagoda	752-4535-11	FDA UDI	Class II	Unknown
Pagoda	158-3500-01A	FDA UDI	Class II	Active
Entrada Hip Stem	510-1210	FDA UDI	Class II	Active
Vusion CS Plus	159-1610-00A	FDA UDI	Class II	Active
Vusion OS	551-7111	FDA UDI	Class II	Unknown
Pagoda	752-8540-12A	FDA UDI	Class II	Active
Solitude Unipolar	132-0041	FDA UDI	Class II	Active
Vusion CS Plus	159-1607-07	FDA UDI	Class II	Unknown
BKS TriMax PS Plus	166-8518	FDA UDI	Class II	Active
Escalade Acetabular System	171-3660	FDA UDI	Class II	Active
Balanced Knee System	163-5520	FDA UDI	Class II	Active
BKS E-Vitalize	166-7211	FDA UDI	Class II	Active
Balance Knee Revision System	566-1415	FDA UDI	Class II	Active
Escalade Acetabular System	170-2864	FDA UDI	Class II	Active
Legend	172-3256	FDA UDI	Class II	Active
Pagoda	158-3035B	FDA UDI	Class II	Active
Pagoda	752-8545-12A	FDA UDI	Class II	Active
Balanced Knee Revision System	562-4400	FDA UDI	Class II	Active
Escalade Acetabular System	171-4062	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.