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Zimmer Trabecular Metal Technology, Inc.

Last updated September 17, 2026

Information

Country: US
Address: 10 POMEROY RD., Parsippany, NJ, 07054
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005751028
DUNS Number: —

Catalogue (895)

Page 16 of 18

Device	Model / Reference	Registries	Class	Status
Trabecular Metal™	06-155-10601	FDA UDI	Class II	Active
Mergence™-S	96-108-50041	FDA UDI	Class II	Active
Vista®-S	06-402-02111	FDA UDI	Class II	Active
Trabecular Metal™	06-165-01121	FDA UDI	Class II	Active
Nexgen® Trabecular Metal™	00-5444-056-36	FDA UDI	Class II	Active
Trabecular Metal™	06-131-20142	FDA UDI	Class II	Active
Vista®-S	06-401-05111	FDA UDI	Class II	Active
Trabecular Metal™	06-101-03111	FDA UDI	Class II	Active
Bigliani/Flatow® Trabecular Metal™	00-4326-040-46	FDA UDI	Class II	Active
Mergence™-S	96-101-04041	FDA UDI	Class II	Active
TM Ardis® Trabecular Metal™	06-701-03131	FDA UDI	Class II	Active
Vista®-S	06-401-02041	FDA UDI	Class II	Active
Mergence™-S	96-101-01081	FDA UDI	Class II	Active
Trabecular Metal™	00-4894-050-30	FDA UDI	Class II	Active
Trabecular Metal™	06-101-01071	FDA UDI	Class II	Active
Mergence™-S	96-102-04061	FDA UDI	Class II	Active
Mergence™-S	96-102-01091	FDA UDI	Class I	Active
Mergence™-S	96-108-47071	FDA UDI	Class II	Active
Mergence™-S	96-108-60091	FDA UDI	Class II	Active
Trabecular Metal™	06-155-10551	FDA UDI	Class II	Active
Mergence™-S	96-102-03121	FDA UDI	Class II	Active
Trabecular Metal™	06-131-10502	FDA UDI	Class II	Active
TM Ardis® Trabecular Metal™	06-701-04111	FDA UDI	Class II	Active
Mergence™-S	96-102-02081	FDA UDI	Class I	Active
Trabecular Metal™	06-115-00391	FDA UDI	Class II	Active
Mergence™-S	96-102-04081	FDA UDI	Class II	Active
Vista®-S	06-402-04081	FDA UDI	Class II	Active
Mergence™-S	96-105-00002	FDA UDI	Class I	Active
Explant™	00-7052-060-00	FDA UDI	Class I	Active
Trabecular Metal™	06-155-00471	FDA UDI	Class II	Active
Nexgen® Trabecular Metal™	00-5445-055-41	FDA UDI	Class II	Active
Trabecular Metal™	06-136-30131	FDA UDI	Class II	Active
Mergence™-S	96-108-10101	FDA UDI	Class II	Active
Mergence™-S	96-101-03081	FDA UDI	Class II	Active
TM Ardis® Trabecular Metal™	06-701-06101	FDA UDI	Class II	Active
Vista®-S	06-401-06101	FDA UDI	Class II	Active
Trabecular Metal™	06-102-01061	FDA UDI	Class II	Active
Trabecular Metal™	00-5451-013-41	FDA UDI	Class II	Active
Trabecular Metal™	00-5451-022-36	FDA UDI	Class I	Active
Trabecular Metal™	06-101-01061	FDA UDI	Class II	Active
Trabecular Metal™	00-5452-013-35	FDA UDI	Class II	Active
Trabecular Metal™	00-5451-021-35	FDA UDI	Class I	Active
Trabecular Metal™	00-4894-066-15	FDA UDI	Class II	Active
Trabecular Metal™	06-131-10122	FDA UDI	Class II	Active
Nexgen® Trabecular Metal™	00-5490-034-24	FDA UDI	Class II	Active
Trabecular Metal™	00-5451-020-35	FDA UDI	Class II	Active
Vista®-S	06-401-01041	FDA UDI	Class II	Active
Mergence™-S	96-108-50121	FDA UDI	Class II	Active
Nexgen® Trabecular Metal™	00-5878-065-38	FDA UDI	Class II	Active
Nexgen® Trabecular Metal™	00-5444-056-31	FDA UDI	Class II	Active

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FDA Recalls (11)

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
Feb 1, 2019	Z-1006-2019	—	terminated	Potentially comingled, resulting in the product in the box potentially not matching the product on the label
Feb 1, 2019	Z-1005-2019	—	terminated	Potentially comingled, resulting in the product in the box potentially not matching the product on the label
Jul 7, 2016	Z-1892-2017	—	terminated	This field action is being initiated following the firm's discovery of a procedural error in the approval of literature resulting in the undo release of certain content. Information was disseminated to distributors and sales representatives during the 2016 National Sales Meeting held February 17-21, 2016.
Apr 15, 2016	Z-1950-2016	—	terminated	Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Apr 15, 2016	Z-1955-2016	—	terminated	Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Apr 15, 2016	Z-1953-2016	—	terminated	Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Apr 15, 2016	Z-1952-2016	—	terminated	Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Apr 15, 2016	Z-1954-2016	—	terminated	Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Apr 15, 2016	Z-1951-2016	—	terminated	Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Feb 4, 2015	Z-1325-2015	—	terminated	One unit of the 20 mm augments was mislabeled as 5 mm and it was subsequently distributed.
Dec 2, 2014	Z-0851-2015	—	terminated	During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.