Identity
- Trade Name
- The Cutting Edge System FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- Medi-Clinch Grasper tip, single use FDA UDI
- Model / Reference
- 91770 FDA UDI
- Description
- Medi-Clinch Grasper tip, single use FDA UDI
Identifiers
- Catalog Number
- 91770 FDA UDI
- Primary DI / UDI-DI
- 00842102104688 FDA UDI
- 510(k) Number
- K103840 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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: Rigid endoscopic tissue manipulation forceps, single-use
The Cutting Edge System by Flexbar Machine Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscopic tissue manipulation forceps, single-use.
- Standard Clamp Disposable SCD22-1 — Standard Bariatrics · Class II
- MINILAP — TELEFLEX INCORPORATED · Class II
- Direct Drive Reposable Graspers — APPLIED MEDICAL RESOURCES CORP. · Class I
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- ReNew — MICROLINE SURGICAL, INC. · Class II
Cleared under the same submission
K103840 also covers:
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
- Mediflex Laparoscopic Instruments - Reusable Electrodes — FLEXBAR MACHINE CORP.
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
- Flexbar Machine Corp.
Sources (1)
- FDA UDI 74a474ed-0ac4-4899-931e-e7d8f3410432 35 fields · synced May 30, 2026