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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 5 of 12

Device	Model / Reference	Registries	Class	Status
B-P Total Hip System	01-01-0560	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0214	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-5248	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0614	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3248	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1502	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0862	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0419	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0612	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0054	FDA UDI	Class II	Active
B-P Total Hip System	01-02-3260	FDA UDI	Class II	Unknown
B-P Total Knee System	04-33-0113	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0620	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-0244	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-01-0001	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0804	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-03-0044	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0815	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-04-0612	FDA UDI	Class II	Active
B-P Total Hip System	01-04-0409	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2844	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0163	FDA UDI	Class II	Active
B-P Total Knee System	04-31-2006	FDA UDI	Class II	Unknown
B-P Total Hip System	01-04-0115	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3256	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1005	FDA UDI	Class II	Active
B-P Total Hip System	01-02-2852	FDA UDI	Class II	Active
B-P Total Hip System	01-01-0552	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3254	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1204	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-04-0108	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0104	FDA UDI	Class II	Active
B-P Total Hip System	01-14-1528	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0812	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-2854	FDA UDI	Class II	Unknown
B-P Total Hip System	01-17-3239	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0818	FDA UDI	Class II	Active
B-P Total Shoulder System	02-03-0056	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0406	FDA UDI	Class II	Active
B-P Total Knee System	04-34-0001	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0111	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2306	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0624	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0211	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0617	FDA UDI	Class II	Active
B-P Total Hip System	01-02-2850	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-2858	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0822	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0212	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-3848	FDA UDI	Class II	Active

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.