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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 6 of 77

Device	Model / Reference	Registries	Class	Status
Pisces Spinal System	753-8560-10A	FDA UDI	Class II	Active
BKS® Uni	763-5062A	FDA UDI	Class II	Active
BKS E-Vitalize	166-7314	FDA UDI	Class II	Active
BKS® Uni	763-7111A	FDA UDI	Class II	Active
Ibis	752-8555-41A	FDA UDI	Class II	Active
Vusion OS	551-6309A	FDA UDI	Class II	Active
Trivicta	513-1209	FDA UDI	Class II	Active
Escalade Acetabular System	170-0140	FDA UDI	Class II	Active
BKS E-Vitalize	166-5218	FDA UDI	Class II	Active
Balanced Knee System	163-5208	FDA UDI	Class II	Active
BKS® Uni	762-5200	FDA UDI	Class II	Active
BKS TriMax PS Plus	166-8118	FDA UDI	Class II	Active
Pagoda	752-8550-31A	FDA UDI	Class II	Active
Envision	154-6316	FDA UDI	Class II	Unknown
Kasm	669-2070	FDA UDI	Class II	Active
Legend	175-3260	FDA UDI	Class II	Active
BKS® Uni	763-1102	FDA UDI	Class II	Active
Pagoda	752-8530-31	FDA UDI	Class II	Unknown
Legend	174-2864	FDA UDI	Class II	Active
Integrated Spine System	158-6530-01	FDA UDI	Class II	Unknown
Vusion PS	551-5209	FDA UDI	Class II	Unknown
Envision	154-5349	FDA UDI	Class II	Unknown
Pagoda	752-5545-31A	FDA UDI	Class II	Active
BKS® Uni	763-1082	FDA UDI	Class II	Active
Ibis Xl	752-9575-57A	FDA UDI	Class II	Active
Balance Knee Revision System	567-5104	FDA UDI	Class II	Active
Balanced Knee System	163-2411	FDA UDI	Class II	Active
Balanced Knee System	163-5716	FDA UDI	Class II	Active
Balanced Knee Revision System	569-1808	FDA UDI	Class II	Active
Legend Acetabular Shell	170-0570	FDA UDI	Class II	Active
Balanced Knee System	163-3108	FDA UDI	Class II	Active
Vusion CS Plus	159-1209-07	FDA UDI	Class II	Unknown
BKS E-Vitalize	166-6414	FDA UDI	Class II	Active
Balanced Knee System	163-1614	FDA UDI	Class II	Active
Escalade Acetabular System	171-3654	FDA UDI	Class II	Active
BKS E-Vitalize	166-5612	FDA UDI	Class II	Active
Balanced Knee System	163-2512	FDA UDI	Class II	Active
BKS TriMax PS Plus	166-8316	FDA UDI	Class II	Active
Vusion OS	551-7614	FDA UDI	Class II	Unknown
BKS TriMax PS Plus	166-8610	FDA UDI	Class II	Active
Vusion OS	551-6514	FDA UDI	Class II	Unknown
Vusion CS Plus	159-1211-07	FDA UDI	Class II	Unknown
Balance Knee Revision System	561-1501	FDA UDI	Class II	Active
Balanced Knee System	161-3401A	FDA UDI	Class II	Active
Ibis	752-7535-41A	FDA UDI	Class II	Active
Ibis	752-4545-26A	FDA UDI	Class II	Active
Pagoda	752-6560-11A	FDA UDI	Class II	Active
Vusion TS	551-5216	FDA UDI	Class II	Unknown
Pivot Bipolar	133-2246	FDA UDI	Class II	Active
Envision	154-5120	FDA UDI	Class II	Unknown

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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.