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ENDOTEC, INC.

Last updated May 23, 2026

Information

Country: US
Address: —
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 803488357

Catalogue (580)

Page 7 of 12

Device	Model / Reference	Registries	Class	Status
B-P Total Hip System	01-17-2849	FDA UDI	Class II	Active
B-P Total Shoulder System	02-02-5348	FDA UDI	Class II	Active
B-P Total Knee System	04-31-1501	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2103	FDA UDI	Class II	Active
B-P Total Knee System	04-31-1102	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2101	FDA UDI	Class II	Active
B-P Total Hip System	01-34-0032	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0100	FDA UDI	Class II	Active
B-P Total Hip System	01-02-4558	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0548	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0119	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2857	FDA UDI	Class II	Unknown
B-P Total Hip System	01-21-0116	FDA UDI	Class II	Active
B-P Total Hip System	01-02-2848	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0114	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0063	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2104	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2506	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-2452	FDA UDI	Class II	Active
B-P Total Hip System	01-03-0042	FDA UDI	Class II	Unknown
B-P Total Hip System	01-14-2028	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0324	FDA UDI	Class II	Unknown
B-P Total Knee System	04-34-0603	FDA UDI	Class II	Active
B-P Total Shoulder System	02-15-0604	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0412	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0301	FDA UDI	Class II	Unknown
B-P Total Hip System	01-04-0413	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0420	FDA UDI	Class II	Active
B-P Total Shoulder System	02-02-5448	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0719	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1201	FDA UDI	Class II	Active
B-P Total Hip System	01-34-1032	FDA UDI	Class II	Active
B-P Total Hip System	01-04-0411	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2843	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0011	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0410	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0314	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0717	FDA UDI	Class II	Active
B-P Total Hip System	01-02-2856	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0136	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0864	FDA UDI	Class II	Active
B-P Total Hip System	01-04-0113	FDA UDI	Class II	Active
B-P Total Knee System	04-34-0002	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0614	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0024	FDA UDI	Class II	Unknown
B-P Total Hip System	01-04-0412	FDA UDI	Class II	Active
B-P Total Hip System	01-02-2846	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0415	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3255	FDA UDI	Class II	Unknown
B-P Total Hip System	01-03-0051	FDA UDI	Class II	Unknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Recalls (20)

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
Sep 21, 2011	Z-0441-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0440-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0432-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0433-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0438-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0436-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0434-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0443-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0437-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0435-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0431-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0439-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Sep 21, 2011	Z-0442-2012	—	terminated	On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee). The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.
Jun 5, 2009	Z-1622-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
Jun 5, 2009	Z-1623-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
Jun 5, 2009	Z-1626-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
Jun 5, 2009	Z-1621-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
Jun 5, 2009	Z-1625-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
Jun 5, 2009	Z-1627-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
Jun 5, 2009	Z-1624-2010	—	terminated	Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.