Registered with FDA
Wise Instruments Inc
Houston, TX, United States. Lists 12 dental device types with FDA across 1 registered establishment.
- Device types listed
- 12
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Wise Instruments Inc currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Dental Hand InstrumentsDZN · Class 1 | Dental hand instruments | Lister | — | 2019 |
| All Types RetractorEIG · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Crown RemoverEIS · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Periodontic ProbeEIX · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Dental Instrument HandleEJB · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Cartridge SyringeEJI · Class 2 | Dental needles & syringes | Lister | — | 2022 |
| Surgical HemostatEMD · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Surgical Tooth Extractor ForcepsEMG · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Surgical Rongeur ForcepsEMH · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Dental Surgical ElevatorEMJ · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Periodontic ScalerEMN · Class 1 | Dental hand instruments | Lister | — | 2022 |
| Orthodontic PlierJEX · Class 1 | Dental hand instruments | Lister | — | 2022 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| WISE INSTRUMENTS INCFDA reg. 3015397788 | Houston, TX, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10060956). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.