# R.H. Electronics Ltd. (contract manufacturer, Nof Hagalil Northern, IL): 6 new FDA device listings, incl. over-the-counter radiofrequency coagulation device for wrinkle reducti

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | R.H. Electronics Ltd. |
| Owner / operator | R. H. Electronics Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Nof Hagalil Northern, IL |
| New listings | 6 |
| Devices | Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction; Massager, Therapeutic, Electric; Stimulator, Muscle, Powered, For Muscle Conditioning; Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption |
| Product codes | PAY, ISA, NGX, OHV |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, Physical Medicine |
| Brand names | (5) GENEO X U with TriPollar RF PRO APPLICATOR KIT for GENEO X U; (2) GENEO X U PACKED with GENEO X TRIPOLLAR KIT USA PACKED; 4) Glo2Facial By Geneo RF PRO Handpiece Kit for GENEO X; (1) GENEO X ELITE System with TriPollar RF and Oxygeneo Applicators; (3) RF PRO Handpiece for GENEO X; (4) Glo2Facial By Geneo RF PRO Handpiece Kit for GENEO X;; (3) RF PRO Handpiece for GENEO X; |
| First new listing | 2026-06-29 |
| Latest new listing | 2026-07-07 |
| FDA registration number | 3005238200 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.