Identity
- Trade Name
- Expasyl FDA UDI
- Generic Name
- Dental impression material syringe, reusable FDA UDI
- Device Name
- Temporary Gingival Retraction System - 40 Applicator Tips FDA UDI
- Model / Reference
- 31173 FDA UDI
- Description
- Temporary Gingival Retraction System - 40 Applicator Tips FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10841396117050 FDA UDI
- FDA Product Code
- MVL FDA UDI
- GMDN Term
- Dental impression material syringe, reusable FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Category: Dental impression material syringe, reusable
Expasyl by Kerr Corporation — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental impression material syringe, reusable.
- Plasdent — PLASDENT CORP. · Class I
- Plasdent — PLASDENT CORP. · Class I
- Plasdent — PLASDENT CORP. · Class I
- Astek — Young Innovations, Inc. · Class I
- COE SYRINGE — Gc America Inc. · Class I
- Astek — Young Innovations, Inc. · Class I
- MASTER-DENT — DENTONICS, INC.
- MASTER-DENT — DENTONICS, 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 U | Pending data |
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Manufacturer
- Manufacturer
- Kerr Corporation
Sources (1)
- FDA UDI 6a560339-b453-421e-be0f-c9782888e850 34 fields · synced Jun 8, 2026