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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 11 of 12

Device	Model / Reference	Registries	Class	Status
B-P Total Hip System	01-03-0041	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-01-0002	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-03-0040	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1301	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0805	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2105	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0813	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0325	FDA UDI	Class II	Unknown
B-P Total Hip System	01-03-0039	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0570	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1104	FDA UDI	Class II	Unknown
B-P Total Hip System	01-04-0108	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0817	FDA UDI	Class II	Active
B-P Total Shoulder System	02-02-0344	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2852	FDA UDI	Class II	Unknown
B-P Total Hip System	01-14-2032	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0056	FDA UDI	Class II	Active
B-P Internal Fixation Accessories	03-01-0615	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0012	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0556	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0021	FDA UDI	Class II	Active
B-P Total Knee System	04-33-0115	FDA UDI	Class II	Active
B-P Total Knee System	04-34-0604	FDA UDI	Class II	Active
B-P Total Hip System	01-02-2854	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2002	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-01-0004	FDA UDI	Class II	Unknown
B-P Total Knee System	04-34-0204	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0423	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-3950	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0216	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1006	FDA UDI	Class II	Active
B-P Total Hip System	01-17-2856	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0102	FDA UDI	Class II	Active
B-P Internal Fixation Accessories	03-01-0640	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0113	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0015	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0462	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0217	FDA UDI	Class II	Active
B-P Total Knee System	04-31-2204	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0825	FDA UDI	Class II	Active
B-P Total Hip System	01-14-0532	FDA UDI	Class II	Unknown
B-P Total Hip System	01-14-1532	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0050	FDA UDI	Class II	Active
B-P Total Knee System	04-34-0202	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-5456	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0046	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0811	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0113	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-21-0103	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0316	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.