Is this your brand? Sign in to claim ownership.

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 4 of 12

Device	Model / Reference	Registries	Class	Status
B-P Total Hip System	01-01-0064	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0306	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0619	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0605	FDA UDI	Class II	Active
B-P Total Knee System	04-31-1106	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-15-0601	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0863	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-04-0608	FDA UDI	Class II	Active
B-P Total Shoulder System	02-21-0204	FDA UDI	Class II	Active
B-P Total Hip System	01-03-0038	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0514	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-4760	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0303	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0115	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-5266	FDA UDI	Class II	Active
B-P Total Knee System	04-31-1302	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0162	FDA UDI	Class II	Active
B-P Total Knee System	04-31-1004	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0326	FDA UDI	Class II	Unknown
B-P Total Hip System	01-16-0820	FDA UDI	Class II	Unknown
B-P Total Hip System	01-02-3262	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0014	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0218	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0562	FDA UDI	Class II	Unknown
B-P Total Hip System	01-01-0546	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-21-0202	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0364	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0604	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0466	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-0452	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0801	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0123	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0425	FDA UDI	Class II	Unknown
B-P Total Hip System	01-04-0114	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0314	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0313	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0112	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0066	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0661	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-2001	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0064	FDA UDI	Class II	Unknown
B-P Total Knee System	04-32-0366	FDA UDI	Class II	Active
B-P Total Knee System	04-32-0323	FDA UDI	Class II	Unknown
B-P Total Shoulder System	02-02-2344	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0112	FDA UDI	Class II	Unknown
B-P Total Knee System	04-33-0132	FDA UDI	Class II	Unknown
B-P Total Knee System	04-34-0602	FDA UDI	Class II	Active
B-P Total Hip System	01-16-0317	FDA UDI	Class II	Active
B-P Total Hip System	01-01-0558	FDA UDI	Class II	Unknown
B-P Total Knee System	04-31-1305	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.