OEM & ODM
Pen Injector Solutions
Customized for your drug, dose and delivery requirements. Start Your Project →Products
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Products Display
Multiple platforms for different drugs and dosing requirements.
Reusable
Reusable Pen Injector Platform for 3 mL Cartridges
Documented 3 mL platform · application-specific variants
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Reusable · 3 mL
80-Unit Reusable Metal Injection Pen Platform
Replaceable-cartridge, adjustable-dose configuration
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Disposable · 3 mL
60-Unit Disposable Peptide Injection Pen
0.01 mL increment · 0.60 mL documented maximum
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Dual-Chamber · 4 mL
Disposable Dual-Chamber Injection Pen
0.01–0.50 mL documented range for powder-and-solvent programs
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Auto Injector
Prefilled Automatic Pen Injector Assembly
Three-step, fixed-dose platform for 1.0 mL slender PFS
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OEM & ODM Configuration
Cartridge, dose system, device architecture and appearance.
Quality evidence
Certifications
FDA 510(k) records A manufacturing partner of ours holds two US FDA 510(k) clearances for pen injector devices — K240774 and K240961, both granted in 2024. Unlike a redacted certificate, these are public records you can look up yourself. Check the records →
Customization Case Showcase
Metal finishesFive color directionsAnodized body colors prepared for visual and finish review
Metal finishesOpen component reviewBody cap and mechanism
Metal finishesWarm finish comparisonGold and orange samples
Metal finishesBrand color setGreen blue white red and black
Metal finishesOpen sample reviewExternal and internal presentation
Metal finishesPaired finish samplesSurface and control comparison
Metal finishesUpright sample setFinish consistency review
Metal finishesHandheld sample checkReal scale and mechanism view
Plastic structuresBody structure optionsHousing colors and cartridge window layouts for project review
Plastic structuresWhite housing sampleHandheld pre shipment check
Plastic structuresCompact body sampleSize and grip review
Plastic structuresMechanism visibilityInternal travel review
Dose identificationColor coded controlsButtons and display surrounds distinguish device configurations
Dose identificationPrinted scale optionsVariant specific presentation
Dose identificationScale and color variantsVisual differentiation
Dose identificationScale window reviewAppearance and reading check
Samples and deliveryFitted sample packagingDevice insert accessory positions and instructions prepared together
Samples and deliveryPresentation kitDevice and accessory layout
Samples and deliveryBatch color checkPacked sample consistency
Samples and deliveryProtected samplesPre shipment packing
Manufacturing
Where these platforms are produced
Penacta is an OEM and ODM partner. The facility below belongs to the manufacturing partner that builds these platforms, and the figures are the partner's facility figures. We re-confirm them with you during supplier qualification.
10,600 m²Cleanroom and production area
2Assembly lines
20+Patents and qualifications
These are photographs of the partner facility. Facility figures are self-reported by the manufacturing partner and are not an audit result, a certification, or a statement that a specific device configuration is approved in your market. Original certificates, audit reports and current facility evidence are shared during qualification.
Working with us
How a first project usually starts
These are the commitments we work to. They are not customer quotations, and we do not publish named references without written permission.
Your drug presentation or device type, the primary container, the dose range you need and your target market. Nothing confidential at this stage.
The documented configurations that could fit, the values that stay configuration-specific, and the questions that must be answered before a quotation means anything.
We will not confirm drug–device compatibility, quote a regulatory clearance, or blend parameters from different variants to make a fit look closer than it is.
Sample, artwork and tooling scope are quoted as separate commercial items, so a first order does not hide its setup cost.
Drawings, verification inputs and certificates are released as the project reaches the stage where they can be released, under an agreed confidentiality route.
Your drug presentation or device type, the primary container, the dose range you need and your target market. Nothing confidential at this stage.
The documented configurations that could fit, the values that stay configuration-specific, and the questions that must be answered before a quotation means anything.
We will not confirm drug–device compatibility, quote a regulatory clearance, or blend parameters from different variants to make a fit look closer than it is.
Sample, artwork and tooling scope are quoted as separate commercial items, so a first order does not hide its setup cost.
Drawings, verification inputs and certificates are released as the project reaches the stage where they can be released, under an agreed confidentiality route.