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Ebi, LLC

Last updated September 17, 2026

Information

Country: US
Address: 1 Gatehall Rd., PARSIPPANY, NJ, 07054
Website: biomet.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 1.973.299.9300
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2242816
DUNS Number: 050410323

Catalogue (168)

Page 1 of 4

Device	Model / Reference	Registries	Class	Status
Biomet SpinalPak / OrthoPak	1067724-1	FDA UDI	Class III	Active
BESTic Healing Abutment	SHAR502	FDA UDI	Class II	Active
CCM UCLA Abutment (for BESTic) [Non-Octa]	EBCUB	FDA UDI	Class II	Unknown
Biomet SpinalPak / OrthoPak	106130-14	FDA UDI	Class III	Active
Biomet EBI Bone Healing System	1068225	FDA UDI	Class III	Active
SpF XL IIb Implantable Spinal Fusion Stimulator	10-1335M	FDA UDI	Class III	Active
Precision II Implant	IRSS3313	FDA UDI	Class II	Active
External Implant (3I type)	EE3M3310H	FDA UDI	Class II	Active
Precision II Implant	IRSS4807	FDA UDI	Class II	Active
BLT II Implant	BLOS4812	FDA UDI	Class II	Active
Biomet OrthoPak Non-invasive Bone Growth Stimulator System	1067727	FDA UDI	Class III	Active
SpF®-XL IIb Implantable Spinal Fusion Stimulator	10-1335W	FDA UDI	Class III	Active
Precision II Implant	IRSS3310	FDA UDI	Class II	Active
Precision II Implant	IWSS4814	FDA UDI	Class II	Active
External Implant (3i type)	EE3R4011H	FDA UDI	Class II	Active
BLT OS Impression Coping	ONOICM	FDA UDI	Class II	Active
BLT II Implant	BLOS4111	FDA UDI	Class II	Active
Precision II Implant	IRSS4107	FDA UDI	Class II	Active
Biomet EBI Bone Healing System	1068236	FDA UDI	Class III	Active
Biomet SpinalPak / OrthoPak	106130-17	FDA UDI	Class III	Active
Precision II Implant	IRSS3314	FDA UDI	Class II	Active
BLT II Implant	BLOS4113T	FDA UDI	Class II	Active
BestDuo Abutment	NOA525	FDA UDI	Class II	Active
External Implant (3i type)	EE3R4013H	FDA UDI	Class II	Active
Precision II Implant	IRSS4112	FDA UDI	Class II	Active
Biomet SpinalPak / OrthoPak	1067720	FDA UDI	Class III	Active
Biomet SpinalPak / OrthoPak	1067724-5	FDA UDI	Class III	Active
Biomet SpinalPak / OrthoPak	1067724-3	FDA UDI	Class III	Active
Reficio DBM Plus	20900321	FDA UDI	Class II	Active
External Implant (3i type)	EE3W5010H	FDA UDI	Class II	Active
Biomet SpinalPak / OrthoPak	1067724-2	FDA UDI	Class II	Active
Biomet SpinalPak / OrthoPak	1067722	FDA UDI	Class II	Active
BLT External Implant(SLA)	BLERS4108	FDA UDI	Class II	Active
Reficio DBM Paste	20700221	FDA UDI	Class II	Active
Biomet SpinalPak / OrthoPak	1067728-1	FDA UDI	Class II	Active
Biomet OrthoPak Non-invasive Bone Growth Stimulator System	1067718-63	FDA UDI	Class III	Active
Biomet SpinalPak / OrthoPak	1067721	FDA UDI	Class II	Active
CCM UCLA Abutment (for Precision) [Non-Octa]	EICUB	FDA UDI	Class II	Unknown
Lindemann Guide Drill	OMD2835	FDA UDI	Class I	Active
BLT II Implant	BLOS4811	FDA UDI	Class II	Active
Biomet EBI Bone Healing System	1068215	FDA UDI	Class II	Active
Loading Lindemann Guide Drill	LLDL	FDA UDI	Class I	Active
EBI OsteoGen™ Implantable Bone Growth Stimulator	10-1328S	FDA UDI	Class III	Active
Precision II Implant	IRSS4111	FDA UDI	Class II	Active
Biomet EBI Bone Healing System	1068209	FDA UDI	Class III	Active
Reficio DBM Paste	20700321	FDA UDI	Class II	Active
Precision II Implant	IRSS3309	FDA UDI	Class II	Active
Biomet EBI Bone Healing System	1068224	FDA UDI	Class III	Active
Precision Gold UCLA Abutment	EIGUC	FDA UDI	Class II	Active
Biomet SpinalPak / OrthoPak	1067723	FDA UDI	Class III	Active

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FDA Recalls (14)

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
Mar 22, 2024	Z-1619-2024	—	open, classified	Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
Mar 22, 2024	Z-1617-2024	—	open, classified	Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
Mar 22, 2024	Z-1616-2024	—	open, classified	Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
Mar 22, 2024	Z-1618-2024	—	open, classified	Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
Nov 11, 2014	Z-0874-2015	—	terminated	A design deficiency was discovered whereby the Drill/Awl Sleeve and Spring-Loaded Drill/Awl Sleeve instruments (the Sleeves) allow the mating Drill and Awl instruments to penetrate 1.0 mm beyond their intended depths during screw hole preparation.
Oct 8, 2014	Z-0909-2015	—	terminated	Inoperative screw head seat splay and/or fracture as a result of positioning of the rod which is a part of the Cypher MIS Screw System.
May 15, 2014	Z-1811-2014	—	terminated	The Cypher MIS Screw Inserter may exhibit an increased rate of instrument tip failure.
Sep 24, 2013	Z-0411-2014	—	terminated	Biomet received a complaint on 5/20/2013 reporting that the tip of the instrument sheared off during a removal case.
Aug 22, 2013	Z-0359-2014	—	terminated	Polaris Translation Screw Failures were recently reported to Biomet Spine. These failures are generally described as dissociation of the screw head from the shaft of the Polaris Translation Screw.
Aug 13, 2013	Z-2214-2013	—	terminated	Several complaints were reported to exhibit screw head splay in the Cypher MIS Screw System.
Apr 9, 2013	Z-2292-2013	—	terminated	Several complaints were recorded regarding one of the three screws driving through the cage of the Solitaire 35 implant.
Feb 7, 2013	Z-0954-2013	—	terminated	Increased risk of failure at the driver tip during screw insertion or removal.
Sep 29, 2012	Z-0536-2013	—	terminated	Broken screw insertor hardness was measured and found to be below the acceptable limits.
Sep 16, 2010	Z-0131-2011	—	terminated	One of the two connector ends of the medium cross connector may not be fully secured to the rod after tightening. This may not be readily apparent to the operating surgeon, resulting in inadequate torsional stability.