Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
- Device Name
- ROBERTS ANG 2MM CUP FCPS 50CM FDA UDI
- Model / Reference
- IPN007783 FDA UDI
- Description
- ROBERTS ANG 2MM CUP FCPS 50CM FDA UDI
Identifiers
- Catalog Number
- 505123 FDA UDI
- Primary DI / UDI-DI
- 24026704530704 FDA UDI
- 510(k) Number
- K990561 FDA UDI
- FDA Product Code
- JEK FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4680 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 50 Centimeter FDA UDI
Category: Surgical soft-tissue manipulation forceps, alligator, reusable
Pilling by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical soft-tissue manipulation forceps, alligator, reusable.
- Integra® — Integra LifeSciences Production Corporation · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- Symmetry Goodhill — SYMMETRY SURGICAL INC. · Class I
- JEDMED — JEDMED Instrument Company · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Micro laryngeal forceps — Spiggle & Theis Medizintechnik GmbH · Class I
- Symmetry Jako — SYMMETRY SURGICAL INC. · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
Cleared under the same submission
K990561 also covers:
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
- PILLING — TELEFLEX INCORPORATED
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
- Teleflex Incorporated
Sources (1)
- FDA UDI afb8de3f-3c74-40a6-80fa-5d8d8a11daf3 37 fields · synced May 30, 2026