Identity
- Trade Name
- Compress Device FDA UDI
- Generic Name
- Orthopaedic bone pin, non-bioabsorbable FDA UDI
- Model / Reference
- 178404 FDA UDI
Identifiers
- Catalog Number
- 178404 FDA UDI
- Primary DI / UDI-DI
- 00880304002890 FDA UDI
- FDA Product Code
- MEH FDA UDIKRO FDA UDIKWY FDA UDILZO FDA UDIKWZ FDA UDIJDI FDA UDILPH FDA UDI
- GMDN Term
- Orthopaedic bone pin, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3353 FDA UDI888.3510 FDA UDI888.3390 FDA UDI888.3310 FDA UDI888.3350 FDA UDI888.3358 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Orthopaedic bone pin, non-bioabsorbable
Compress Device by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic bone pin, non-bioabsorbable.
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- IlluminOss — ILLUMINOSS MEDICAL INC. · Class II
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Cleared under the same submission
K031804 also covers:
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
K043547 also covers:
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- COMPRESS DEVICE — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, Inc.
- Compress Device — Biomet Orthopedics, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 307858a9-1273-4319-89fe-f36841c71e15 36 fields · synced Jun 6, 2026