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Titanium Blade Super Slide II Self Retaining Retractor, Extended Set
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Titanium Blade Super Slide II Self Retaining Retractor, Extended Set FDA UDI
- Generic Name
- Self-retaining surgical retractor, reusable FDA UDI
- Device Name
- Titanium Blade Super-Slide II Basic Retractor Set Extended Consists of the Following: 1x 7329-10, 4x 7329-82, 4x 7329-84, 4x 7329-86 4x 7329-87 and 2x 7329-60 2x 7329-62 2x 7329-68 1x 7329-90 FDA UDI
- Model / Reference
- 7329-09 FDA UDI
- Description
- Titanium Blade Super-Slide II Basic Retractor Set Extended Consists of the Following: 1x 7329-10, 4x 7329-82, 4x 7329-84, 4x 7329-86 4x 7329-87 and 2x 7329-60 2x 7329-62 2x 7329-68 1x 7329-90 FDA UDI
Identifiers
- Catalog Number
- 7329-09 FDA UDI
- Primary DI / UDI-DI
- 10840199500687 FDA UDI
- 510(k) Number
- K881160 FDA UDI
- FDA Product Code
- GZT FDA UDI
- GMDN Term
- Self-retaining surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Self-retaining surgical retractor, reusable
Titanium Blade Super Slide II Self Retaining Retractor, Extended Set by Koros USA, Inc. — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Self-retaining surgical retractor, reusable.
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class I
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Symmetry Cloward — SYMMETRY SURGICAL INC. · Class II
- Life Instruments — Life Instrument Corporation · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- SELF RETAINING CORONOID RETRACTOR CHAIN WITH RINGS — W.H. Holden, Inc. · Class I
Cleared under the same submission
K881160 also covers:
- All Titanium Super Slide III Self Retaining Retractor, Extended Set — Koros USA, Inc.
- Clear View S-Slide II Instrument Case — Koros USA, Inc.
- Clearview Super Slide Lumbar Retractor, Basic Set — Koros USA, Inc.
- Double Crank Spinal Blade — Koros USA, Inc.
- Double Crank Spinal Retractor Frame, McElroy Stainless Steel — Koros USA, Inc.
- S-Slide All Titanium Wide Blade Retractor Frame — Koros USA, Inc.
- Super Slide II Self Retaining Retractor, Extended Set — Koros USA, Inc.
- Super Slide III Ti Retractor Frame — Koros USA, Inc.
- Super Slide Titanium 1" Wide Blade Radiolucent Retractor Set — Koros USA, Inc.
- Super-Slide 1" Wide Blade — Koros USA, Inc.
- Super-Slide 1" Wide Blade — Koros USA, Inc.
- Super-Slide 1" Wide Titanium Blade — Koros USA, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Koros USA, Inc.
Sources (1)
- FDA UDI a230f9b1-97b2-4fe3-bf16-33bf520fdd1e 37 fields · synced May 30, 2026