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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 2 of 12

Device	Model / Reference	Registries	Class	Status
B-P Total Hip System	01-04-0408	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2005	FDA UDI	Class II	Active
B-P Total Hip System	01-21-0112	FDA UDI	Class II	Active
B-P Total Hip System	01-01-0554	FDA UDI	Class II	Unknown
B-P Total Knee System	04-33-0114	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-0252	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0145	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0621	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0026	FDA UDI	Class II	Active
B-P Total Knee System	04-31-2504	FDA UDI	Class II	Active
B-P Total Shoulder System	02-04-0610	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0815	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2851	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0102	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0712	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1002	FDA UDI	Class II	Active
B-P Total Hip System	01-21-0111	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0118	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2003	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0513	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2853	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0812	FDA UDI	Class II	Active
B-P Total Hip System	01-03-0047	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-21-0203	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0417	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0362	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-5252	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0625	FDA UDI	Class II	Active
B-P Total Hip System	01-04-0416	FDA UDI	Class II	Unknown
B-P Total Knee System	04-33-0122	FDA UDI	Class II	Active
B-P Total Hip System	01-02-3258	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0070	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2206	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0106	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0609	FDA UDI	Class II	Unknown
B-P Total Knee System	04-34-0201	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1203	FDA UDI	Class II	Active
B-P Total Hip System	01-02-5164	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3258	FDA UDI	Class II	Unknown
B-P Internal Fixation Accessories	03-01-0650	FDA UDI	Class II	Active
B-P Total Shoulder System	02-15-0602	FDA UDI	Class II	Active
B-P Total Shoulder System	02-04-0112	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-04-0212	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0312	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0365	FDA UDI	Class II	Active
B-P Total Shoulder System	02-02-0248	FDA UDI	Class II	Unknown
B-P Total Hip System	01-21-0113	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0013	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2201	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2305	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.