Is this your brand? Sign in to claim ownership.

Zimmer Orthopaedic Surgical Products

Last updated May 23, 2026

What Zimmer Orthopaedic Surgical Products makes

Zimmer Orthopaedic Surgical Products manufactures surgical saw blades (oscillating and reciprocating, single-use), surgical pneumatic tourniquet systems, surgical helmet systems, sequential venous compression system inflators, dermatome handpieces, leg procedure positioners, and surgical fluid/smoke waste management system suction units.

The company's portfolio includes Class I and Class II devices, which are listed in the FDA Unique Device Identifier (UDI) registry. Zimmer Orthopaedic Surgical Products is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Zimmer Orthopaedic Surgical Products manufacture?

Where is Zimmer Orthopaedic Surgical Products based?

Zimmer Orthopaedic Surgical Products is based in the United States, as indicated by the country information provided in the device data.

Which regulatory registries list Zimmer Orthopaedic Surgical Products' devices?

Zimmer Orthopaedic Surgical Products' devices are listed in the FDA Unique Device Identifier (UDI) registry, as specified in the device data provided.

How are Zimmer Orthopaedic Surgical Products' devices classified?

Zimmer Orthopaedic Surgical Products manufactures Class I and Class II devices, which are lower-risk medical devices compared to Class III devices, as indicated in the device data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (1346)

Page 2 of 27

Device	Model / Reference	Registries	Class	Status
H.a.s.®	00-2555-030-05	FDA UDI	Class II	Unknown
Stablecut®	14041060LMX	FDA UDI	Class I	Active
Stablecut®	25090127YX1	FDA UDI	Class I	Active
Stablecut®	506120	FDA UDI	Class I	Active
Stablecut®	223000270	FDA UDI	Class I	Active
A.T.S.® Personalized Pressure®	60-2200-301-05	FDA UDI	Class I	Active
ActiveCare	ActiveCare calf large sleeve with stockinette	FDA UDI	Class II	Active
Stablecut®	48060064ALJ	FDA UDI	Class I	Active
Stablecut®	25090137YB1	FDA UDI	Class I	Active
Stablecut®	506090	FDA UDI	Class I	Active
Totalshield® Ii	00992000600	FDA UDI	Class II	Active
Stablecut®	13070119AL1	FDA UDI	Class I	Active
Stablecut®	32-700390	FDA UDI	Class I	Active
Totalshield®	00-9900-310-10	FDA UDI	Class II	Active
Stablecut®	25090127AD1	FDA UDI	Class I	Active
Stablecut®	14041060LMX	FDA UDI	Class I	Active
Stablecut®	11-2884	FDA UDI	Class I	Active
Stablecut®	25090137AV1	FDA UDI	Class I	Active
Stablecut®	13090137XF1	FDA UDI	Class I	Active
Stablecut®	506125	FDA UDI	Class I	Active
Hemovac® Wound Drainage System	00-1500-005-10	FDA UDI	Class I	Unknown
Stablecut®	25070147XG1	FDA UDI	Class I	Active
Stablecut®	19090089XF1	FDA UDI	Class I	Active
Stablecut®	11-3769	FDA UDI	Class I	Active
Stablecut®	25-0901-37Y-TB	FDA UDI	Class I	Active
Stablecut®	13090119AF1	FDA UDI	Class I	Active
Stablecut®	25090119AD1	FDA UDI	Class I	Active
Stablecut®	09025060AMF	FDA UDI	Class I	Active
Stablecut®	13070137YL1	FDA UDI	Class I	Active
Stablecut®	20038127YA1	FDA UDI	Class I	Active
Stablecut®	21090100YL1	FDA UDI	Class I	Active
Stablecut®	17100119LGS	FDA UDI	Class I	Active
Stablecut®	25105137AG1	FDA UDI	Class I	Active
Stablecut®	20105127AGC	FDA UDI	Class I	Active
Stablecut®	25090127DG1	FDA UDI	Class I	Active
Stablecut®	13065119XG1	FDA UDI	Class I	Active
Stablecut®	25090127XTB	FDA UDI	Class I	Active
A.T.S.® Personalized Pressure®	60-2200-301-08	FDA UDI	Class I	Active
Stablecut®	25090127AV1	FDA UDI	Class I	Active
Stablecut®	506133	FDA UDI	Class I	Active
Stablecut®	06078100LRL	FDA UDI	Class I	Active
Totalshield®	00-9910-301-12	FDA UDI	Class II	Active
ActiveCare® DVT	A502B000102	FDA UDI	Class II	Active
Stablecut®	21090127YV1	FDA UDI	Class I	Active
Stablecut®	25100127YX1	FDA UDI	Class I	Active
Stablecut®	25090147XX1	FDA UDI	Class I	Active
Stablecut®	11-2607	FDA UDI	Class I	Active
Hemovac® Wound Drainage System	00-1500-060-10	FDA UDI	Class I	Unknown
Stablecut®	13070137LL1	FDA UDI	Class I	Active
Stablecut®	11-3749	FDA UDI	Class I	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 (15)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Zimmer Orthopaedic Surgical Products has 15 recall records, with the earliest initiated on 2004-10-27 and the most recent on 2007-12-18. All recalls have been terminated. The reasons given include port/tube bond separation in cuffs during surgery and compromised sterility due to silicone stain effects on Tyvek lids.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

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.