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ORTHO DEVELOPMENT CORP.

Last updated September 17, 2026

What ORTHO DEVELOPMENT CORP. makes

Ortho Development Corp. manufactures orthopedic implants including tibial inserts, acetabular shells, knee and hip prostheses (both uncoated and coated, modular and fixed), spinal bone screws, polymeric spinal interbody fusion cages, and knee arthroplasty wedges. Specific device examples include the Pagoda, Balance Knee Revision System, BKS TriMax PS Plus, Trivicta, Escalade Acetabular System, BKS E-Vitalize, and BKS® Uni.

All listed devices are classified as Class II medical devices and are registered in the FDA’s Unique Device Identification (fda_udi) system. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Ortho Development Corp. make?

Ortho Development Corp. manufactures orthopedic implants such as tibial inserts, acetabular shells, knee and hip prostheses (both uncoated and coated, modular and fixed), spinal bone screws, polymeric spinal interbody fusion cages, and knee arthroplasty wedges. Specific examples include the Pagoda, Balance Knee Revision System, BKS TriMax PS Plus, Trivicta, Escalade Acetabular System, BKS E-Vitalize, and BKS® Uni.

Where is Ortho Development Corp. based?

Ortho Development Corp. is based in the United States, as stated in the provided device data under the COUNTRY field.

Which registries list Ortho Development Corp.'s devices?

Ortho Development Corp.'s devices are listed in the FDA’s Unique Device Identification (fda_udi) system, as indicated in the LISTED IN field of the device data.

How are Ortho Development Corp.'s devices classified?

All devices manufactured by Ortho Development Corp. are classified as Class II medical devices, as explicitly stated in the DEVICE CLASSES field of the provided data.

AI-generated from registry data and not verified by a human reviewer.

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 55 of 77

Device	Model / Reference	Registries	Class	Status
BKS® Uni	763-5071	FDA UDI	Class II	Active
Balanced Knee Revision System	563-2720	FDA UDI	Class II	Active
Pagoda	752-6550-31	FDA UDI	Class II	Unknown
Legend Acetabular Shell	170-0664	FDA UDI	Class II	Active
Balance Knee Revision System	567-2105	FDA UDI	Class II	Active
Balanced Knee Revision System	563-2310	FDA UDI	Class II	Active
Vusion TS	551-1114	FDA UDI	Class II	Unknown
Pagoda	752-6540-11	FDA UDI	Class II	Unknown
Balanced Knee Revision System	563-2412	FDA UDI	Class II	Active
Ibis	752-7560-41	FDA UDI	Class II	Unknown
Vusion OS	551-6213	FDA UDI	Class II	Unknown
Alpine Hip System	700-1020	FDA UDI	Class II	Active
Balanced Knee System Revision	567-7101A	FDA UDI	Class II	Active
Legend	173-2844	FDA UDI	Class II	Active
Balanced Knee Revision System	563-2210	FDA UDI	Class II	Active
Balanced Knee Revision System	568-2402	FDA UDI	Class II	Active
Balanced Knee System	163-1407	FDA UDI	Class II	Active
BKS TriMax PS Plus	166-8509	FDA UDI	Class II	Active
Delta Ceramic Femoral Head	136-4060	FDA UDI	Class II	Active
Legend	172-3250	FDA UDI	Class II	Active
Vusion OS	551-7209	FDA UDI	Class II	Unknown
Balanced Knee System	163-3311	FDA UDI	Class II	Active
Balanced Knee Revision System	565-1211	FDA UDI	Class II	Active
Trivicta	513-0212	FDA UDI	Class II	Active
Envision	154-6314	FDA UDI	Class II	Unknown
Vusion PS	551-2013	FDA UDI	Class II	Unknown
Pagoda	158-3075-01	FDA UDI	Class II	Unknown
Vusion OS	551-7514	FDA UDI	Class II	Unknown
Delta Ceramic Femoral Head	136-3213	FDA UDI	Class II	Active
BKS® Uni	763-4061A	FDA UDI	Class II	Active
BKS E-Vitalize	166-6111	FDA UDI	Class II	Active
Balanced Knee Revision System	569-1115	FDA UDI	Class II	Active
Vusion TS	551-5014	FDA UDI	Class II	Unknown
Pagoda	752-5530-11A	FDA UDI	Class II	Active
Balanced Knee System	161-3701	FDA UDI	Class II	Active
BKS TriMax	165-1201	FDA UDI	Class II	Active
Balanced Knee Revision System	567-7207	FDA UDI	Class II	Active
Ibis	752-5555-41A	FDA UDI	Class II	Active
BKS E-Vitalize	166-7508	FDA UDI	Class II	Active
Vusion CS Plus	159-1608-00	FDA UDI	Class II	Unknown
Balance Knee Revision System	567-2202	FDA UDI	Class II	Active
Integrated Spine System	158-3080	FDA UDI	Class II	Unknown
Ibis	752-5540-26A	FDA UDI	Class II	Active
Pagoda	752-6570-31A	FDA UDI	Class II	Active
Trivicta	513-0011	FDA UDI	Class II	Active
BKS® Uni	763-6062A	FDA UDI	Class II	Active
Ibis Xl	752-7595-57A	FDA UDI	Class II	Active
Pagoda	158-3200-01	FDA UDI	Class II	Unknown
Balanced Knee System	163-1514	FDA UDI	Class II	Active
Pagoda	752-8535-31A	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

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Authorities

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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.

There are 28 recall records for Ortho Development Corp., with the earliest initiated on December 26, 2002, and the most recent on May 30, 2019. The statuses of these recalls include open, classified, and terminated. The reasons given for the recalls include erroneous lot numbers, potential mechanical issues such as restricted movement or breakage of components, incorrect assembly, improper sealing of foil pouches, mislabeling, and manufacturing defects affecting fit or function.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

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.