Identity
- Trade Name
- MECRON™ Washer FDA UDI
- Generic Name
- Implantable bone washer FDA UDI
- Model / Reference
- for 4.0 headed screws FDA UDI
Identifiers
- Catalog Number
- CH15048 FDA UDI
- Primary DI / UDI-DI
- 04048266168337 FDA UDI
- 510(k) Number
- K172213 FDA UDI
- FDA Product Code
- HTN FDA UDI
- GMDN Term
- Implantable bone washer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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: Implantable bone washer
MECRON™ Washer by Merete GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Implantable bone washer.
- ISOLA — Depuy Spine, Inc. · Class II
- Spiked Gridlock Screw Washer — Trilliant Surgical LLC · Class II
- Monster Screw System — Paragon 28 · Class II
- ALPHALOK Plating System — Vilex, Inc. · Class II
- Monster Screw System — Paragon 28 · Class II
- FLAT WASHER — Biomet Orthopedics, Inc. · Class II
- Fixcet Spinal Facet Screw System — Xtant Medical Holdings, Inc. · U
- LEOS Cannulated Screw System — Tyber Medical · Class II
Cleared under the same submission
K172213 also covers:
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
- MECRON™ Cannulated Screw — Merete GmbH
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
- Merete GmbH
Sources (1)
- FDA UDI 2ac2b219-8bb6-4e69-b68e-2b329cd87d7f 35 fields · synced Jun 8, 2026