Registered with FDA

Peak Implements Inc

South River, NJ, United States. Lists 13 dental device types with FDA across 1 registered establishment.

FDA owner/operator10059019Repacker / relabeler
Device types listed
13
Brands and models
13
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Peak Implements Inc currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Mouth MirrorEAX · Class 1Dental hand instrumentsLister
MIRROR, MOUTH
2020
Orthodontic Band PusherECS · Class 1Dental hand instrumentsLister
PUSHER, BAND, ORTHODONTIC
2021
Dental Dressing ForcepsEFL · Class 1Dental hand instrumentsLister
FORCEPS, DRESSING, DENTAL
2020
Dental Surgical Tissue ScissorsEGN · Class 1Dental hand instrumentsLister
SCISSORS, SURGICAL TISSUE, DENTAL
2020
All Types RetractorEIG · Class 1Dental hand instrumentsLister
RETRACTOR, ALL TYPES
2020
Dental Instrument Depth GaugeEIL · Class 1Dental hand instrumentsLister
GAUGE, DEPTH, INSTRUMENT, DENTAL
2021
Collar and Crown ScissorsEIR · Class 1Dental hand instrumentsLister
SCISSORS, COLLAR AND CROWN
2020
Periodontic ProbeEIX · Class 1Dental hand instrumentsLister
PROBE, PERIODONTIC
2020
Dental Instrument HandleEJB · Class 1Dental hand instrumentsLister
HANDLE, INSTRUMENT, DENTAL
2020
Operative ExplorerEKB · Class 1Dental hand instrumentsLister
EXPLORER, OPERATIVE
2020
Surgical Tooth Extractor ForcepsEMG · Class 1Dental hand instrumentsLister
FORCEPS, TOOTH EXTRACTOR, SURGICAL
2020
Periodontic ScalerEMN · Class 1Dental hand instrumentsLister
SCALER, PERIODONTIC
2020
Orthodontic PlierJEX · Class 1Dental hand instrumentsLister
PLIER, ORTHODONTIC
2020

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

EstablishmentLocationWhat it does
PEAK IMPLEMENTS INCFDA reg. 3015176311South River, NJ, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10059019). 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.