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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 10 of 12

Device	Model / Reference	Registries	Class	Status
B-P Total Knee System	04-32-0124	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0209	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1503	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2850	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0022	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-3252	FDA UDI	Class II	Active
B-P Total Knee System	04-31-1306	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2839	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0861	FDA UDI	Class II	Active
B-P Total Hip System	01-01-0048	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0509	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0422	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0363	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0402	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0103	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2847	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0220	FDA UDI	Class II	Unknown
B-P Total Knee System	04-33-0105	FDA UDI	Class II	Active
B-P Total Hip System	01-02-3266	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2102	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0061	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0665	FDA UDI	Class II	Unknown
B-P Total Hip System	01-21-0109	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-2248	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0613	FDA UDI	Class II	Active
B-P Total Hip System	01-17-3245	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0824	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0124	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0566	FDA UDI	Class II	Unknown
B-P Total Knee System	04-34-0605	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0603	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0616	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2858	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3243	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-5444	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2840	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0416	FDA UDI	Class II	Active
B-P Total Knee System	04-31-2303	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0819	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-2448	FDA UDI	Class II	Active
B-P Total Hip System	01-14-0032	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2203	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0116	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0068	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2855	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0622	FDA UDI	Class II	Unknown
B-P Total Knee System	04-33-0126	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0161	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0517	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0403	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.