Identity
- Trade Name
- No-Scalpel Vasectomy FDA UDI
- Generic Name
- Surgical penis clamp, reusable FDA UDI
- Device Name
- No-Scalpel Vasectomy Ring Clamp, 3.5mm FDA UDI
- Model / Reference
- 3.5mm clamp FDA UDI
- Description
- No-Scalpel Vasectomy Ring Clamp, 3.5mm FDA UDI
Identifiers
- Catalog Number
- LV-3CL-857 FDA UDI
- Primary DI / UDI-DI
- 15055515600261 FDA UDI
- FDA Product Code
- KOA FDA UDI
- GMDN Term
- Surgical penis clamp, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4730 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 3.5 Millimeter FDA UDI
Category: Surgical penis clamp, reusable
No-Scalpel Vasectomy by Femcare , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical penis clamp, reusable.
- GEN2 — SURGIX MEDICAL LLC · Class I
- American Medicals — AMERICAN MEDICALS · Class I
- STOCKMANN PENIS FORCEPS — SONTEC INSTRUMENTS, INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- AESCULAP — AESCULAP, INC. · Class II
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Femcare , Ltd.
Sources (1)
- FDA UDI 927c9d5f-e0df-49b4-9112-7e8864fb8ab6 35 fields · synced May 30, 2026