Ophthalmic Forceps K5-7500
Ophthalmic Forceps K5-7500 is a Class I device made by Katena Products, Inc., listed in FDA GUDID since 14 Sep 2020 (UDI-DI 00841668107348), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841668107348 | Date14 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00841668107348
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ophthalmic Forceps
- Generic name
- Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
- Model / Ref / Catalog
- K5-7500
- Primary DI / UDI-DI
- 00841668107348
- FDA product code
- HNR
- GMDN term
- Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
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