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Zimmer Orthopaedic Surgical Products

Last updated May 23, 2026

Information

Country: US
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Catalogue (1346)

Page 1 of 27

Device	Model / Reference	Registries	Class	Status
Stablecut®	25090137XCW	FDA UDI	Class I	Active
Stablecut®	11-2835	FDA UDI	Class I	Active
Stablecut®	21090137XFW	FDA UDI	Class I	Active
Stablecut®	20090137AGC	FDA UDI	Class I	Active
Stablecut®	20100127AVC	FDA UDI	Class I	Active
Stablecut®	08075100AF1	FDA UDI	Class I	Active
Stablecut®	506114	FDA UDI	Class I	Active
Stablecut®	18090137YX1	FDA UDI	Class I	Active
Stablecut®	19105127AG1	FDA UDI	Class I	Active
Stablecut®	19090089LF1	FDA UDI	Class I	Active
H.a.s.®	00-2555-050-05	FDA UDI	Class II	Active
Stablecut®	11-2954	FDA UDI	Class I	Active
Stablecut®	25095127XB1	FDA UDI	Class I	Active
Stablecut®	21090137LV1	FDA UDI	Class I	Active
Stablecut®	11-3259	FDA UDI	Class I	Active
Stablecut®	25095119XB1	FDA UDI	Class I	Active
Stablecut®	13100089YF1	FDA UDI	Class I	Active
Stablecut®	11-2912	FDA UDI	Class I	Active
Stablecut®	07031060XTC	FDA UDI	Class I	Active
Stablecut®	13090147YF1	FDA UDI	Class I	Active
Stablecut®	25090137AD1	FDA UDI	Class I	Active
Stablecut®	11-3204	FDA UDI	Class I	Active
Stablecut®	19090137YG1	FDA UDI	Class I	Active
Stablecut®	11-3771	FDA UDI	Class I	Active
Stablecut®	25090147AB1	FDA UDI	Class I	Active
Stablecut®	25075119YT1	FDA UDI	Class I	Active
Stablecut®	18090127XX1	FDA UDI	Class I	Active
Stablecut®	25090127CG1	FDA UDI	Class I	Active
Hemovac® Wound Drainage System	00-1500-050-10	FDA UDI	Class I	Unknown
Stablecut®	19090119YG1	FDA UDI	Class I	Active
A.T.S.® Personalized Pressure®	60-4000-301-10	FDA UDI	Class I	Active
Stablecut®	13090127LF1	FDA UDI	Class I	Active
Stablecut®	20100119AVC	FDA UDI	Class I	Active
Stablecut®	13070147AL1	FDA UDI	Class I	Active
Stablecut®	25090100AF1	FDA UDI	Class I	Active
Stablecut®	13090089AF1	FDA UDI	Class I	Active
A.T.S.® Personalized Pressure®	60-2200-301-07	FDA UDI	Class I	Active
Stablecut®	11-3764	FDA UDI	Class I	Active
Stablecut®	14041060SMX	FDA UDI	Class I	Active
Stablecut®	19105137LG1	FDA UDI	Class I	Active
Stablecut®	06078100SRL	FDA UDI	Class I	Active
Stablecut®	25090119AGC	FDA UDI	Class I	Active
Stablecut®	30065089AL1	FDA UDI	Class I	Active
Stablecut®	06048119SRL	FDA UDI	Class I	Active
Stablecut®	18100147XX1	FDA UDI	Class I	Active
Stablecut®	13105127YF1	FDA UDI	Class I	Active
Stablecut®	19100137XG1	FDA UDI	Class I	Active
Stablecut®	506109	FDA UDI	Class I	Active
Stablecut®	25090127LV1	FDA UDI	Class I	Active
Stablecut®	18090119YX1	FDA UDI	Class I	Active

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FDA Recalls (15)

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
Dec 18, 2007	Z-0864-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0863-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0860-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0865-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0857-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0861-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0862-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0859-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0856-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Dec 18, 2007	Z-0858-2008	—	terminated	Sterility (package integrity) compromised; The effect of a silicone stain produced during assembly operations on the sterility barrier properties of the Tyvek lids has not been validated by the firm.
Feb 11, 2005	Z-0565-05	—	terminated	The port/tube bond in the affected cuffs may separate during surgery causing the pressure in the cuff to release.
Feb 11, 2005	Z-0564-05	—	terminated	The port/tube bond in the affected cuffs may separate during surgery causing the pressure in the cuff to release.
Oct 27, 2004	Z-0388-05	—	terminated	The port/tube bond in the affected cuffs may separate during surgery causing the pressure in the cuff to release.
Oct 27, 2004	Z-0390-05	—	terminated	The port/tube bond in the affected cuffs may separate during surgery causing the pressure in the cuff to release.
Oct 27, 2004	Z-0389-05	—	terminated	The port/tube bond in the affected cuffs may separate during surgery causing the pressure in the cuff to release.