Identity
- Trade Name
- Tonsil Sponges FDA UDI
- Generic Name
- Dissection sponge FDA UDI
- Device Name
- Tonsil Sponges 1.25" X-Large FDA UDI
- Model / Reference
- 50-02 FDA UDI
- Description
- Tonsil Sponges 1.25" X-Large FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20749915000760 FDA UDI
- 510(k) Number
- K872806 FDA UDI
- FDA Product Code
- EFQ FDA UDI
- GMDN Term
- Dissection sponge FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dissection sponge
Tonsil Sponges by American Surgical Company, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K872806 also covers:
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 U | Pending data |
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Manufacturer
- Manufacturer
- American Surgical Company, LLC
Sources (1)
- FDA UDI 49c9db91-408d-4860-a4e0-a9c11687372c 34 fields · synced Jun 9, 2026