Glaukos HF5
by Katena Products, Inc. United States GUDID
Product code HKS
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10841668146580 | Date15 Jan 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Glaukos
- Generic Name
- Gonioscope
- Model / Ref / Catalog
- HF5
- Primary DI / UDI-DI
- 10841668146580
- FDA Product Code
- HKS
- GMDN Term
- Gonioscope
- Device Class
- Class I
- Regulation Number
- 886.1660
- Commercial Distribution
- In Commercial Distribution
Other devices from Katena Products, Inc.
Properties & raw data
Show properties, registry sources and raw records
Other properties (9)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 983c671d-97e2-4fc0-9856-82572ec2aac3