Identity
- Trade Name
- A Link Z FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- Small Oblique Retainer FDA UDI
- Model / Reference
- 10-000034 FDA UDI
- Description
- Small Oblique Retainer FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810043480017 FDA UDI
- 510(k) Number
- K201671 FDA UDI
- FDA Product Code
- OVD FDA UDI
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 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
No
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical screwdriver, reusable
A Link Z by Acuity Surgical Devices, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical screwdriver, reusable.
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- LOSPA IS Spinal Fixation System — Corentec Co., Ltd · Class II
- PERLA ® TL — Spineart · Class II
- USS — Synthes · Class I
- Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class I
- CosmoLock Pedicle Screw System — Kalitec Direct LLC · Class I
Cleared under the same submission
K201671 also covers:
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
- A Link Z — ACUITY SURGICAL DEVICES, LLC
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Acuity Surgical Devices, Llc
Sources (1)
- FDA UDI 8e49043c-1470-4251-89b5-6b60c133113d 35 fields · synced May 31, 2026